Supplementary Information. Catalytic reductive cleavage of methyl -D-glucoside acetals to ethers using hydrogen as a clean reductant

Similar documents
Directed Studies Towards The Total Synthesis of (+)-13-Deoxytedanolide: Simple and Convenient Synthesis of C8-C16 fragment.

Suzuki-Miyaura Coupling of NHC-Boranes: a New Addition to the C-C Coupling Toolbox

SUPPLEMENTARY MATERIAL

Metal-Free One-Pot α-carboxylation of Primary Alcohols

SUPPLEMENTARY INFORMATION. SYNTHESIS OF NEW PYRAZOLO[1,5-a]QUINAZOLINE DERIVATES

SUPPORTING INFORMATION

Dithiocarbonic acid S-{[(1-tert-butylcarbamoyl-propyl)-prop-2-ynylcarbamoyl]-methyl}

Palladium Catalyzed Amination of 1-Bromo- and 1-Chloro- 1,3-butadienes: a General Method for the Synthesis of 1- Amino-1,3-butadienes

Visible light promoted thiol-ene reactions using titanium dioxide. Supporting Information

Base catalyzed sustainable synthesis of phenyl esters from carboxylic acids using diphenyl carbonate

Enantioselective Synthesis of ( )-Jiadifenin, a Potent Neurotrophic Modulator

Insight into the complete substrate-binding pocket of ThiT by chemical and genetic mutations

Regioselective C-H bond functionalizations of acridines. using organozinc reagents

Cobalt-catalyzed reductive Mannich reactions of 4-acryloylmorpholine with N-tosyl aldimines. Supplementary Information

Electronic Supplementary Material (ESI) for RSC Advances This journal is The Royal Society of Chemistry 2013

Phosphine oxide-catalyzed dichlorination reactions of. epoxides

Eugenol as a renewable feedstock for the production of polyfunctional alkenes via olefin cross-metathesis. Supplementary Data

Supporting information. for. Highly Stereoselective Synthesis of Primary, Secondary and Tertiary -S-Sialosides under Lewis Acidic Conditions

2-Hydroxyindoline-3-triethylammonium Bromide: A Reagent for Formal C3-Electrophilic Reactions of. Indoles

Supporting Information

An Environment-Friendly Protocol for Oxidative. Halocyclization of Tryptamine and Tryptophol Derivatives

Zn-mediated electrochemical allylation of aldehydes in aqueous ammonia

Supporting Information

Supplementary data. A Simple Cobalt Catalyst System for the Efficient and Regioselective Cyclotrimerisation of Alkynes

Supporting Information Reaction of Metalated Nitriles with Enones

Supporting Information

Stereoselective Synthesis of Tetracyclic Indolines via Gold-Catalyzed Cascade Cyclization Reactions

A simple, efficient and green procedure for Knoevenagel condensation catalyzed by [C 4 dabco][bf 4 ] ionic liquid in water. Supporting Information

Experimental Section. General information

A New Acyl Radical-Based Route to the 1,5- Methanoazocino[4,3-b]indole Framework of Uleine and Strychnos Alkaloids

SUPPORTING INFORMATION

Supporting Information. for. Z-Selective Synthesis of γ,δ-unsaturated Ketones via Pd-Catalyzed

Design of NIR Chromenylium-Cyanine Fluorophore Library for Switch-ON and Ratiometric Detection of Bio-Active Species in Vivo

Nitro-enabled catalytic enantioselective formal umpolung alkenylation of β-ketoesters

Four-Component Reactions towards Fused Heterocyclic Rings

Supporting Information

Supporting Information

Near IR Excitation of Heavy Atom Free Bodipy Photosensitizers Through the Intermediacy of Upconverting Nanoparticles

Enantioselective Synthesis of Cyclopropylcarboxamides using s- BuLi/Sparteine-Mediated Metallation

Supporting Information. Improved syntheses of high hole mobility. phthalocyanines: A case of steric assistance in the

Gold-catalyzed domino reaction of a 5-endo-dig cyclization and [3,3]-sigmatropic rearrangement towards polysubstituted pyrazoles.

Synthesis of imidazolium-based ionic liquids with linear and. branched alkyl side chains

Supporting Information

Gold(I)-Catalyzed Formation of Dihydroquinolines and Indoles from N-Aminophenyl propargyl malonates

Desymmetrization of 2,4,5,6-Tetra-O-benzyl-D-myo-inositol for the Synthesis of Mycothiol

Preparation of N-substituted N-Arylsulfonylglycines and their Use in Peptoid Synthesis

Supporting Information

Supporting Information

Supporting Information

Supporting Information

First enantioselective synthesis of tetracyclic intermediates en route to madangamine D

Preparation of allylboronates by Pd-catalyzed borylative cyclization of dienynes

Exerting Control over the Acyloin Reaction

General Synthesis of Alkenyl Sulfides by Palladium-Catalyzed Thioetherification of Alkenyl Halides and Tosylates

Pyridine Activation via Copper(I)-Catalyzed Annulation toward. Indolizines

Enantioselective total synthesis of fluvirucinin B 1

Total Synthesis of Sphingofungin F by Orthoamide-Type Overman Rearrangement of an Unsaturated Ester. Supporting Information

Supporting Information. Novel fatty acid methyl esters from the actinomycete

Supporting Information. Small molecule inhibitors that discriminate between protein arginine N- methyltransferases PRMT1 and CARM1

Diborane Heterolysis: Breaking and Making B-B bonds at Magnesium

Electronic Supplementary Information for

Supporting Information

Electronic Supporting Information. Optimisation of a lithium magnesiate for use in the noncryogenic asymmetric deprotonation of prochiral ketones

SmI 2 H 2 O-Mediated 5-exo/6-exo Lactone Radical Cyclisation Cascades

Synthesis of diospongin A, ent-diospongin A and C-5 epimer of diospongin B from tri-o-acetyl-d-glucal

Supporting information for. Modulation of ICT probability in bi(polyarene)-based. O-BODIPYs: Towards the development of low-cost bright

Phosphorylated glycosphingolipids essential for cholesterol mobilization in C. elegans

Squaric acid: a valuable scaffold for developing antimalarials?

Stereoselective Synthesis of the CDE Ring System of Antitumor Saponin Scillascilloside E-1

Organic & Biomolecular Chemistry

Structure and reactivity in neutral organic electron donors derived from 4-dimethylaminopyridine

Regio- and Stereoselective Aminopentadienylation of Carbonyl Compounds. Orgánica (ISO), Universidad de Alicante, Apdo. 99, Alicante, Spain.

Performance. Reliability. Productivity. Automated Flash Chromatography Systems

Customer Responsibilities. Important Customer Information Infinity LC/1260 Infinity LC Site Preparation Checklist

New Guanidinium-based Room-temperature Ionic Liquids. Substituent and Anion Effect on Density and Solubility in Water

NMR. picospin. Maintenance Guide

Electronic supplementary information for Light-MPEG-assisted organic synthesis

Discovery of antagonists of PqsR, a key player in 2-alkyl-4-quinolone-dependent quorum sensing in Pseudomonas aeruginosa.

CHM-201 General Chemistry and Laboratory I Unit #3 Take Home Test Due April 18, 2018

Supporting Information

Speed Performance Reliability. Medicinal Chemistry Natural Products Peptides & Polymers Organic Synthesis Purifications

Betti reaction enables efficient synthesis of 8-hydroxyquinoline inhibitors of 2-oxoglutarate. Contents Compound Characterisation...

Synthesis of an Advanced Intermediate of the Jatrophane Diterpene Pl 4: A Dibromide Coupling Approach

Supporting Information

IMPORTANT MANUSCRIPT SUBMISSION REQUIREMENTS

CHM-201 General Chemistry and Laboratory I Unit #3 Unit Test Version A April 18, CORRECTED

Tips and Tricks Part-II: Bits and pieces

OTHER FEATURES UNIQUE FEATURES

Assay Creosote Extraction of Selected Posts from the 1958 Cooperative Test After 50 Years of Exposure as a Ground Contact Preservative

Customer Responsibilities. Important Customer Information. Agilent InfinityLab LC Series Site Preparation Checklist

CHM-201 General Chemistry and Laboratory I Unit #3 Unit Test Version B April 18, 2018 CORRECTED

Supporting Information for Effectiveness of Global, Low-Degree Polynomial Transformations for GCxGC Data Alignment

Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai , China

This article appeared in a journal published by Elsevier. The attached copy is furnished to the author for internal non-commercial research and

IMPORTANT MANUSCRIPT SUBMISSION REQUIREMENTS

HPLC Tips and Tricks. Tiziana Ladisa Sales Support Specialist for Chromatography Italy Thermo Fisher Scientific, Rodano (MI)

One-Pot Synthesis of Symmetric 1,7-Dicarbonyl Compounds Via. a Tandem Radical Addition - Elimination Addition Reaction

Chem 203 December 20, Final Exam Part II Problem 1 of 3 (30 points)

Site Specific Protein Immobilization Into Structured Polymer Brushes Prepared by AFM Lithography

Supporting Information

Transcription:

Electronic Supplementary Material (ESI) for RSC Advances. This journal is The Royal Society of Chemistry 24 Supplementary Information Catalytic reductive cleavage of methyl -D-glucoside acetals to ethers using hydrogen as a clean reductant Charlotte Gozlan, a,b Romain Lafon, a Nicolas Duguet, a Andreas Redl b and Marc Lemaire *,a a Laboratoire de CAtalyse SYnthèse et ENvironnement (CASYEN), Institut de Chimie et Biochimie Moléculaires et Supramoléculaires (ICBMS), CNRS, UMR-5246, Université Claude Bernard Lyon, 43 boulevard du novembre 98, Bât. Curien/CPE, 69622, Villeurbanne, France. E-mail: marc.lemaire.chimie@univ-lyon.fr ; Fax: +33-472-43-4-8; Tel: +33-472-43-4-7. b TERES SYRAL SAS, Z.I et Portuaire B.P.32, 6739 Marckolsheim, France. E-mail: andreas.redl@tereos.com ; Tel: +33-388-58-6-5. Table of contents. General information...2 2. Derivatization method...2 3. GC method...2 4. General procedures...3 5. Characterization data...3 5.. Characterization data of methyl -D-glucoside acetals 2a-e...3 5.2. Characterization data of methyl -D-glucoside ethers 3a-e and 4a-e...5 6. H and 3 C NMR spectra...9 6.. H and 3 C spectra of methyl -D-glucoside acetals 2a-e...9 6.2. H and 3 C spectra of methyl -D-glucoside ethers 3a-e and 4a-e...4

. General information Methyl -D-glucoside (> 98% purity) was purchased from Sigma-Aldrich or Alfa-Aesar and Pd/C (5 or %, Pd on activated carbon, reduced and dry, Escat 43) from Strem Chemicals. Valeraldehyde, hexanal, octanal, decanal and dodecanal were supplied by Sigma-Aldrich or Alfa- Aesar. Amberlyst 5 dry was bought from Rohm and Haas. All other reagents and solvents were used as received without further purification. NMR spectra were acquired on a Bruker 3 ( H, 3 MHz; 3 C, 75 MHz) spectrometer at 293 K. Shifts are referenced relative to the CDCl 3 residual peak (δ H : 7.26 ppm; δ C : 77.6 ppm). The chemical shifts (δ) are expressed in ppm and the coupling constants (J) are given in Hz. The following abbreviations used are: s = singlet, d = doublet, t = triplet, dd = doublet of doublets, td = triplet of doublets, m = multiplet, br = broad. Electrospray ionization (ESI) mass spectra (MS) and High-Resolution Mass Spectra (HRMS) were recorded in the positive mode using spectrometer (MicroTFQ-II, Bruker Daltonics, Bremen). Thin-layer chromatography (TLC) was carried out on aluminum sheets coated with silica gel Merck 6 F254 (.25 mm) revealed with a solution of sulfuric acid at v/v% in ethanol. Flash column chromatography was performed with silica gel Merck Si 6 (4 63 μm). Infrared (IR) spectra were recorded in a SMART itr-nicolet is spectrometer using Attenuated Total Reflectance (ATR) and the wavenumbers ( max) are expressed in cm -. Melting points were measured using a Kofler apparatus and noted in C. 2. Derivatization method Prior to analysis, the sample was silylated as follows: the crude mixture was diluted in THF (25mL), then ml of this solution was diluted in.3 ml of the silylating reagent (pyridine:hexamethyldisilazane (HMDS):chlorotrimethylsilane (TMSCl) in v/v/v :.2:. proportions) The mixture was then heated at 7 C and stirred vigorously for min. Then, the sample was diluted in ml of a THF solution containing methyl oleate (internal standard) at.3 g/l. Finally, the sample was filtrated using a syringe filter (PTFE;.2 µm) before injection in GC. 3. GC method Gas chromatography analyses (GC) for the optimization of the hydrogenolysis of methyl -Dglucoside acetals were performed using a Shimadzu GC (GC-225) equipped with a DB-5MS capillary column (3 m,.25 mm i.d,.25 µm film thickness) and a FID as detector. The carrier gas was helium, at a flow rate of.24 ml/min. The column temperature was initially at C, gradually increased to 24 C at 8 C/min and kept at 24 C for 3 min., then gradually increased to 28 C at 8 C/min. and finally kept at 28 C for min. The injector temperature was set at 24 C and the transfer line temperature was at 28 C. C.C. Sweeley, R. Bentley, M. Makita, W.W. Wells, J. Am. Chem. Soc., 963, 85, 2497-257. 2

4. General procedures General procedure for the preparation of methyl α-d-glucoside acetals (A) In a -ml round bottom flask, under an argon atmosphere, methyl -D-glucoside (3.22 g, 6.6 mmol, 2 equiv) was dissolved in dry THF ( ml) with sodium sulfate (.8 g, 2 mmol,.5 equiv) under an argon atmosphere. The aldehyde (8.3 mmol, equiv) was added dropwise over a -min period, followed by Amberlyst 5 (2wt%/aldehyde). The mixture was magnetically stirred at reflux (66 C) for 3 hours. After cooling to room temperature, the reaction mixture was filtered, washed with EtAc (2 25 ml) and the filtrate was concentrated under reduced pressure. The residue was purified by flash chromatography (EtAc:cylohexane) to give methyl 4,6--alkylidene -D-glucoside 2a-e as a single diastereoisomer. General procedure for the reductive cleavage of methyl α-d-glucoside acetals (B) Methyl 4,6--alkylidene -D-glucoside 2a-e (3 mmol) was diluted in dry CPME (3 ml) and 5%- Pd/C (.45 g, 5 mol% in Pd) was added in a -ml stainless steel autoclave. The reactor was tightly closed, purged three times with hydrogen and hydrogen pressure was introduced (3 bar). The system was heated at 2 C and mechanically stirred for 5 hours. After cooling to room temperature, hydrogen pressure was released and the reaction mixture was then dissolved in absolute ethanol ( ml) and filtered (Millipore Durapore filter. µm). The filtrate was evaporated under reduced pressure and the residue was purified by flash chromatography (EtAc/cyclohexane 5:5 to : then EtH/EtAc :9) to give methyl glucoside ethers 3a-e and 4a-e as a colourless oil. GC analysis after silylation revealed a mixture of 4-and 6-ether regioisomers. 5. Characterization data 5.. Characterization data of methyl -D-glucoside acetals 2a-e H 4 7 3 2a 6 5 2 H Me Methyl 4,6--pentylidene -D-glucopyranoside [3744--5] (2a): The title compound was prepared from methyl -D-glucoside (7.49 g, 3 mmol) and valeraldehyde (.64 g, 9 mmol) following the procedure A to give 2a (2.4 g, 43%) as a white solid. Mp = 78 C; H NMR (3 MHz, CDCl 3 ) δ H :.88 (3H, t, J = 7, CH 3 alkyl),.2.44 (4H, m, 2(CH 2 ) alkyl),.52.72 (2H, m, CH 2 alkyl), 2.8 (H, d, J = 9, H 3 ), 3.23 (H, t, J = 9, H 3 ), 3.3 (H, d, J=2, H 2 ), 3.4 (3H, s, CH 3 ), 3.48 (H, t, J=, H 2 ), 2 3.67 (2H, m, H 5 +H 6 ), 3.83 (H, td, J=9 and 2, H 4 ), 4.9 (H, dd, J= and 4, H 6 ), 2 (H, t, J=5, H 7 ), 4.73 (H, d, J=4, H ); 3 C NMR (75 MHz, CDCl 3 ) δ C : (CH 3 alkyl), 22.62 (CH 2 alkyl), 26.3 (CH 2 alkyl), 34.3 (CH 2 alkyl), 54 (CH 3 ), 62.62 (CH 5 ), 67 (CH 26 ), 7.7 (CH 4 ), 72.98 (CH 2 ), 8.47 (CH 3 ), 99.87 (CH ), 2.8 (CH 7 ). IR ν max : 3399 (H), 2956 (-CH 3 ), 2862 (-CH 2 -), 428, 39, 62, 4, 989; HRMS (ESI + ) calcd for C 2 H 22 Na 6 : 285.39 [M+Na] +,found: 285.35 (-2.2 ppm); GC: R t = 5.85 min; Rf =.27 (8:2 EtAc/cyclohexane). 3

H 4 7 3 2b 6 5 2 H Me Methyl 4,6--hexylidene -D-glucopyranoside [23828-42-2] (2b): The title compound was prepared from methyl -D-glucoside (3.22 g, 6.6 mmol) and hexanal (.83 g, 8.3 mmol) following the procedure A to give 2b (.98 g, 43%) as a white solid. Mp = 84 C; H NMR (3 MHz, CDCl 3 ) δ H :.86 (3H, t, J = 7, CH 3 alkyl),.5.3 (4H, m, 2(CH 2 ) alkyl),.3.46 (2H, m, CH 2 alkyl),.52.74 (2H, m, CH 2 alkyl), 3.2 (H, br s, H 3 ), 3.23 (H, t, J = 9, H 3 ), 3.4 (3H, s, CH 3 ), 3.47 (H, t, J=, H 2 ), 2 3.66 (2H, m, H 5 +H 6 ), 3.83 (H, t, J=9, H 4 ), 4.9 (H, dd, J= and 5, H 6 ), 2 (H, t, J=5, H 7 ), 4.72 (H, d, J=4, H ); 3 C NMR (75 MHz, CDCl 3 ) δ C : 4. (CH 3 alkyl), 22.62 (CH 2 alkyl), 23.86 (CH 2 alkyl), 3.74 (CH 2 alkyl), 34.28 (CH 2 alkyl), 5 (CH 3 ), 62.62 (CH 5 ), 66 (CH 26 ), 7.6 (CH 4 ), 72.95 (CH 2 ), 8.49 (CH 3 ), 99.9 (CH ), 2.8 (CH 7 ); IR ν max : 3433 (H), 2925 (-CH 3 ), 286 (-CH 2 -), 465, 379, 6, 983; HRMS (ESI + ) calcd for C 3 H 24 Na 6 : 299.465 [M+Na] + ; found: 299.464 (+.4 ppm); GC: R t = 7.37 min; Rf =.27 (8:2 EtAc/cyclohexane). H 4 7 3 2c 6 5 2 H Me Methyl 4,6--octylidene -D-glucopyranoside [23828-44-4] (2c): The title compound was prepared from methyl -D-glucoside (3.22 g, 6.6 mmol) and octanal (.6 g, 8.3 mmol) following the procedure A to give 2c (.94 g, 37%) as a white solid. Mp = 8 C; H NMR (3 MHz, CDCl 3 ) δ H :.85 (3H, t, J = 7, CH 3 alkyl),.7.3 (8H, m, 4(CH 2 ) alkyl),.32.47 (2H, m, CH 2 alkyl),.5.73 (2H, m, CH 2 alkyl), 3.2 (2H, br s, H 2 +H 3 ), 3.23 (H, t, J = 9, H 3 ), 3.4 (3H, s, CH 3 ), 3.48 (H, t, J=, H 2 ), 2 3.67 (2H, m, H 5 ), 3.83 (H, t, J=9, H 4 ), 4.9 (H, dd, J= and 5, H 6 ), 2 (H, t, J=5, H 7 ), 4.72 (H, d, J=4, H ); 3 C NMR (75 MHz, CDCl 3 ) δ C : 4.8 (CH 3 alkyl), 22.73 (CH 2 alkyl), 24.8 (CH 2 alkyl), 29.26 (CH 2 alkyl), 2 (CH 2 alkyl), 3.85 (CH 2 alkyl), 34.33 (CH 2 alkyl), 53 (CH 3 ), 62.62 (CH 5 ), 66 (CH 26 ), 7.68 (CH 4 ), 72.97 (CH 2 ), 8.48 (CH 3 ), 99.88 (CH ), 2.82 (CH 7 ); IR ν max : 3368 (H), 2924 (-CH 3 ), 2857 (-CH 2 -), 465, 378, 28, 9, 64, 37, 993; HRMS (ESI + ) calcd for C 5 H 28 Na 6 : 327.778 [M+Na] + ; found: 327.78 (-.6 ppm); GC: R t = 9.86 min; Rf =.2 (5:5 EtAc/cyclohexane). H 4 7 3 2d 6 5 2 H Me Methyl 4,6--decylidene -D-glucopyranoside [23828-46-6] (2d): The title compound was prepared from methyl -D-glucoside (2 g, 2 mmol) and decanal (7.97 g, 5 mmol) following the procedure A to give 2d (7.48 g, 44%) as a white solid. Mp = 72 C; H NMR (3 MHz, CDCl 3 ) δ H :.87 (3H, t, J = 7, CH 3 alkyl),.6.32 (2H, m, 6(CH 2 ) alkyl),.33.45 (2H, m, CH 2 alkyl),.55.72 (2H, m, CH 2 alkyl), 2.6 (2H, br s, H 3 +H 2 ), 3.24 (H, t, J = 9, H 3 ), 3.42 (3H, s, CH 3 ), 3.49 (H, t, J=, H 2 ), 3 3.68 (2H, m, H 5 ), 3.84 (H, t, J=9, H 4 ), 4. (H, dd, J= and 5, H 6 ), 3 (H, t, J=5, H 7 ), 4.74 (H, d, J=4, H ); 3 C NMR (75 MHz, CDCl 3 ) δ C : 4.3 (CH 3 alkyl), 29 (CH 2 alkyl), 24.8 (CH 2 alkyl), 29.25 (CH 2 alkyl), 29.46 (CH 2 alkyl), 29.49 (2CH 2 alkyl), 3.82 (CH 2 alkyl), 34.9 (CH 2 alkyl), 55.2 (CH 3 ), 64 (CH 5 ), 68.43 (CH 26 ), 7.9 (CH 4 ), 72.65 (CH 2 ), 3 (CH 3 ),.2 (CH ), 2.64 (CH 7 ); IR ν max : 3393 (H), 2922 (-CH 3 ), 2853 (-CH 2 -), 466, 378, 2, 88, 4

63, 37, 99; HRMS (ESI + ) calcd for C 7 H 32 Na 6 : 355.29 [M+Na] + ; found: 355.22 (-3.2 ppm); GC: R t = 2 min; Rf =.32 (8:2 EtAc/cyclohexane). H 4 7 3 2e 6 5 2 H Me Methyl 4,6--dodecylidene -D-glucopyranoside [2465-69-2] (2e): The title compound was prepared from methyl -D-glucoside (3.22 g, 6.6 mmol) and dodecanal (.52 g, 8.3 mmol) following the procedure A to give 2e (.77 g, 26%) as a white solid. Mp = 69 C; H NMR (3 MHz, CDCl 3 ) δ H :.86 (3H, t, J = 7, CH 3 alkyl),.7.32 (6H, m, 8(CH 2 ) alkyl),.33.47 (2H, m, CH 2 alkyl),.53.74 (2H, m, CH 2 alkyl), 2.85 (2H, br s, H 3 +H 2 ), 3.24 (H, t, J = 9, H 3 ), 3.4 (3H, s, CH 3 ), 3.49 (H, t, J=, H 2 ), 3 3.68 (2H, m, H 5 ), 3.84 (H, t, J=9, H 4 ), 4. (H, dd, J= and 5, H 6 ), 2 (H, t, J=5, H 7 ), 4.74 (H, d, J=4, H ); 3 C NMR (75 MHz, CDCl 3 ) δ C : 4.24 (CH 3 alkyl), 22.8 (CH 2 alkyl), 24.2 (CH 2 alkyl), 29.46 (CH 2 alkyl), 28 (CH 2 alkyl), 29.62 (CH 2 alkyl), 29.67 (CH 2 alkyl), 29.74 (CH 2 alkyl), 29.76 (CH 2 alkyl), 32.3 (CH 2 alkyl), 34.36 (CH 2 alkyl), 57 (CH 3 ), 62.63 (CH 5 ), 67 (CH 26 ), 7.8 (CH 4 ), 73.2 (CH 2 ), 8.46 (CH 3 ), 99.85 (CH ), 2.84 (CH 7 ); IR ν max : 3388 (H), 292 (-CH 3 ), 2852 (-CH 2 -), 466, 378, 89, 63, 37, 99; HRMS (ESI + ) calcd for C 9 H 36 Na 6 : 383.244 [M+Na] + ; found: 383.2398 (+.6 ppm); GC: R t = 25.45 min; Rf =.3 (6:4 EtAc/cyclohexane). 5.2. Characterization data of methyl -D-glucoside ethers 3a-e and 4a-e H H 3a H Me H H 4a H Me Methyl 6--pentyl -D-glucopyranoside (3a) and methyl 4--pentyl -D-glucopyranoside (4a): The title compounds were prepared from methyl -D-glucoside acetal 2a (4. g, 5 mmol) following the procedure B to give a 7:3 mixture of 3a and 4a (.5 g, 38%) as a white paste. The mixture of ethers was purified by column chromatography (EtAc/cyclohexane 5:5 to : then EtH/EtAc :9) for the characterization of each regioisomer. 3a: colourless oil. H NMR (3 MHz, CDCl 3 ) δ H :.84 (3H, t, J = 7, CH 3 alkyl),.4.36 (4H, m, 2(CH 2 ) alkyl),.4.68 (2H, m, CH 2 alkyl), 3.34 (3H, s, CH 3 ), 3.4 3.82 (7H, m), 3 4.8 (4H, m, CH-anomeric + 3H); 3 C NMR (75 MHz, CDCl 3 ) δ C : 4.6 (CH 3 alkyl), 23 (CH 2 alkyl), 28.2 (CH 2 alkyl), 29.29 (CH 2 alkyl), 55.2 (CH 3 ), 7.2 (CH 2 ), 7 (CH), 7.74 (CH), 7.9 (CH), 7 (CH 2 ), 74.26 (CH), 96 (CH-anomeric); IR ν max : 3382 (H), 2929 (-CH 3 ), 286 (-CH 2 -), 455, 363, 92, 44, 8, 4, 9; HRMS (ESI + ) calcd for C 2 H 24 Na 6 : 287.465 [M+Na] + ; found: 287.467 (-.8 ppm); GC: R t = 7.64 min; Rf =.35 (: EtAc/EtH). 4a: colourless oil. H NMR (3 MHz, CDCl 3 ) δ H :.86 (3H, t, J = 7, CH 3 alkyl),.6.38 (4H, m, 2(CH 2 ) alkyl),.42.66 (2H, m, CH 2 alkyl), 3.6 (3H, br s, H), 3.2 (H, t, J = ), 3.37 (3H, s, CH 3 ), 3.42 3.87 (7H, m), 4.7 (H, d, J = 3, CH anomeric); 3 C NMR (75 MHz, CDCl 3 ) δ C : 4. (CH 3 alkyl), 22.6 (CH 2 alkyl), 28.26 (CH 2 alkyl), (CH 2 alkyl), 55.32 (CH 3 ), 6.92 (CH 2 ), 7. (CH), 72.6 (CH), 73.4 (CH 2 ), 72 (CH), 77.86 (CH), 99.35 (CH-anomeric); IR ν max : 3388 (H), 2928 (-CH 3 ), 2852 (-CH 2 -), 452, 37, 92, 83, 37, 93; HRMS (ESI + ) calcd for C 2 H 24 Na 6 : 287.465 [M+Na] + ; found: 287.465 (+.2 ppm); GC: R t = 6.49 min; Rf =.4 (: EtAc/EtH). 5

H H 3b H Me H H 4b H Me Methyl 6--hexyl -D-glucopyranoside (3b) and methyl 4--hexyl -D-glucopyranoside (4b): The title compounds were prepared from methyl -D-glucoside acetal 2b ( g, 2 mmol) following the procedure B to give a 72:28 mixture of 3b and 4b (2.8 g, 37%) as a colourless oil. The mixture of ethers was purified by column chromatography (EtAc/cyclohexane 5:5 to : then EtH/EtAc :9) for the characterization of each regioisomer. 3b: colourless oil. H NMR (3 MHz, CDCl 3 ) δ H :.84 (3H, t, J = 7, CH 3 alkyl),.3.38 (6H, m, 3(CH 2 ) alkyl),.44.64 (2H, m, CH 2 alkyl), 3.38 (3H, s, CH 3 ), 3.39 3.78 (8H, m), 3 (3H, br s, H), 4.7 (H, d, J = 4, CHanomeric); 3 C NMR (75 MHz, CDCl 3 ) δ C : 4. (CH 3 alkyl), 22.66 (CH 2 alkyl), 25.75 (CH 2 alkyl), 29.6 (CH 2 alkyl), 3.75 (CH 2 alkyl), 55.8 (CH 3 ), 7.24 (CH 2 ), 5 (CH), 7.79 (CH), 7.94 (CH), 72.3 (CH 2 ), 74.28 (CH), 96 (CH-anomeric); IR ν max : 3376 (H), 2928 (-CH 3 ), 2859 (-CH 2 - ), 455, 364, 92, 44, 6, 43, 9; HRMS (ESI + ) calcd for C 3 H 26 Na 6 : 3.622 [M+Na] + ; found: 3.62 (+3.3 ppm); GC: R t = 8.82 min; Rf=.32 (: EtAc/EtH). 4b: colourless oil. H NMR (3 MHz, CDCl 3 ) δ H :.87 (3H, t, J = 7, CH 3 alkyl),.7.4 (6H, m, 3(CH 2 ) alkyl),.46.66 (2H, m, CH 2 alkyl), 2.43 2.78 (3H, br s, H), 3.23 (H, t, J = ), 3.39 (3H, s, CH 3 ), 3.48 (H, dd, J = and 4), 3 3.64 (2H, m), 3.64 3.9 (4H, m), 4.73 (H, d, J = 4, CH-anomeric); 3 C NMR (75 MHz, CDCl 3 ) δ C : 4.6 (CH 3 alkyl), 22.72 (CH 2 alkyl), 25.83 (CH 2 alkyl), 3.38 (CH 2 alkyl), 3.8 (CH 2 alkyl), 55.4 (CH 3 ), 6 (CH 2 ), 7. (CH), 72.72 (CH), 73.24 (CH 2 ), 74.8 (CH), 77.9 (CH), 99.27 (CH-anomeric); IR ν max : 3395 (H), 2927 (-CH 3 ), 2852 (-CH 2 -), 456, 365, 92, 4, 27, 896; C 3 H 26 Na 6 : 3.622 [M+Na] + ; found: 3.6 (+4. ppm); GC: R t = 6 min; Rf=.38 (: EtAc/EtH). H H 3c H Me H H 4c H Me Methyl 6--octyl -D-glucopyranoside (3c) and methyl 4--octyl -D-glucopyranoside (4c): The title compounds were prepared from methyl -D-glucoside acetal 2c (5. g, 6.4 mmol) following the procedure B to give a 75:25 mixture of 3c and 4c (2.3 g, 4%) as a colourless oil. The mixture of ethers was purified by column chromatography (EtAc/cyclohexane 5:5 to : then EtH/EtAc :9) for the characterization of each regioisomer. 3c: colourless oil. H NMR (3 MHz, CDCl 3 ) δ H :.86 (3H, t, J = 7, CH 3 alkyl),.5.38 (H, m, 5(CH 2 ) alkyl),.48.68 (2H, m, CH 2 alkyl), 3.4 (3H, s, CH 3 ), 3.42 3.92 (8H, m), 4.22 (3H, br s, H), 4.73 (H, d, J = 4, CHanomeric); 3 C NMR (75 MHz, CDCl 3 ) δ C : 4.22 (CH 3 alkyl), 22.78 (CH 2 alkyl), 2 (CH 2 alkyl), 29.39 (CH 2 alkyl), 29 (CH 2 alkyl), 29.72 (CH 2 alkyl), 3.96 (CH 2 alkyl), 55.3 (CH 3 ), 7.44 (CH 2 ), 7.2 (CH), 72.8 (CH), 72.24 (CH), 74.44 (CH 2 ), 77.36 (CH), 99.6 (CH-anomeric); IR ν max : 337 (H), 2923 (-CH 3 ), 2854 (-CH 2 -), 456, 365, 92, 44, 8, 44, 9; HRMS (ESI + ) calcd for C 5 H 3 Na 6 : 329.935 [M+Na] + ; found: 329.943 (- ppm); GC: R t = 2.92 min; Rf =.26 (: EtAc/EtH). 4c: white solid. H NMR (3 MHz, CDCl 3 ) δ H :.86 (3H, t, J = 7, CH 3 alkyl),.9.39 (H, m, 5(CH 2 ) alkyl),.43.66 (2H, m, CH 2 alkyl), 8 (3H, br s, H), 3.23 (H, t, J = ); 3.39 (3H, s, CH 3 ), 3.48 (H, dd, J = and 4), 3 3.64 (2H, m), 3.66 3.89 (4H, m), 4.73 (H, d, J = 4, CH-anomeric); 3 C NMR (75 MHz, CDCl 3 ) δ C : 4.2 (CH 3 alkyl), 22.76 (CH 2 alkyl), 26.8 (CH 2 alkyl), 29.37 (CH 2 alkyl), 28 (CH 2 alkyl), 3.44 (CH 2 alkyl), 3.93 (CH 2 alkyl), 55.4 (CH 3 ), 62.8 (CH 2 ), 7. (CH), 72.75 (CH), 73.25 (CH 2 ), 74.84 (CH), 77.94 (CH), 99.28 (CH-anomeric); IR 6

ν max : 3388 (H), 2922 (-CH 3 ), 2853 (-CH 2 -), 456, 365, 92, 44,, 45, 899; C 5 H 3 Na 6 : 329.935 [M+Na] + ; found: 329.935 (-.2 ppm); GC: R t = 2.35 min; Rf =.38 (: EtAc/EtH). H H 3d H Me H H 4d H Me Methyl 6--decyl -D-glucopyranoside (3d) and methyl 4--decyl -D-glucopyranoside (4d): (CG478+CG52)The title compounds were prepared from methyl -D-glucoside acetal 2a (6 g, 8 mmol) following the procedure B to give a 77:23 mixture of 3d and 4d (.52 g, 25%) as a white paste. The mixture of ethers was purified by column chromatography (EtAc/cyclohexane 5:5 to : then EtH/EtAc :9) for the characterization of each regioisomer. 3d: colourless oil. H NMR (3 MHz, CDCl 3 ) δ H :.86 (3H, t, J = 7, CH 3 alkyl),..38 (4H, m, 7(CH 2 ) alkyl),.47.66 (2H, m, CH 2 alkyl), 3.4 (3H, s, CH 3 ), 3.42 3.89 (8H, m), 4.32 (3H, br s, H), 4.73 (H, d, J = 4, CH-anomeric); 3 C NMR (75 MHz, CDCl 3 ) δ C : 4.22 (CH 3 alkyl), 22.79 (CH 2 alkyl), 2 (CH 2 alkyl), 29.45 (CH 2 alkyl), 29.65 (CH 2 alkyl), 29.72 (2CH 2 alkyl), 29.74 (CH 2 alkyl), 32.2 (CH 2 alkyl), 55.27 (CH 3 ), 7.4 (CH 2 ), 7.48 (CH), 7.2 (CH), 72.4 (CH), 72.23 (CH 2 ), 74.4 (CH), 99.6 (CH-anomeric); IR ν max : 34 (H), 299 (-CH 3 ), 2852 (-CH 2 -), 467, 369, 23, 43, 4, 9; HRMS (ESI + ) calcd for C 7 H 34 Na 6 : 357.2248 [M+Na] + ; found: 357.2247 (+. ppm); GC: R t = 2 min; Rf =.3 (: DCM/MeH). 4d: white solid. H NMR (3 MHz, CDCl 3 ) δ H :.88 (3H, t, J = 7, CH 3 alkyl),..39 (4H, m, 7(CH 2 ) alkyl),.47.68 (2H, m, CH 2 alkyl), 2.3 (4H, br s, H + H), 3.25 (H, t, J = ); 3.4 (3H, s, CH 3 ), 3.48 (H, dd, J = and 4), 4 3.68 (2H, m), 3.69 3.94 (3H, m), 4.75 (H, d, J = 4, CH-anomeric); 3 C NMR (75 MHz, CDCl 3 ) δ C : 4.25 (CH 3 alkyl), 22.82 (CH 2 alkyl), 26.2 (CH 2 alkyl), 29.45 (CH 2 alkyl), 29.63 (CH 2 alkyl), 29.7 (CH 2 alkyl), 29.73 (CH 2 alkyl), 3.47 (CH 2 alkyl), 32.2 (CH 2 alkyl), 55.47 (CH 3 ), 62.8 (CH 2 ), 7.99 (CH), 72.82 (CH), 73.28 (CH 2 ), 75.8 (CH), 77.95 (CH), 99.9 (CH-anomeric); IR ν max : 337 (H), 2923 (-CH 3 ), 2853 (- CH 2 -), 466, 37, 37, 92, 2, 7, 5, 899; C 7 H 34 Na 6 : 357.2248 [M+Na] + ; found: 357.2252 (-.2 ppm); GC: R t = 23.2 min; Rf =.38 (: EtAc/EtH). H H 3e H Me H H 4e H Me Methyl 6--dodecyl -glucopyranoside (3e) and methyl 4--dodecyl -D-glucopyranoside (4e): The title compounds were prepared from methyl -D-glucoside acetal 2e (5. g, 4 mmol) following the procedure B to give a 73:27 mixture of 3e and 4e (2 g, 5%) as a white solid. The mixture of ethers was purified by column chromatography (EtAc/cyclohexane 5:5 to : then EtH/EtAc :9) for the characterization of each regioisomer. 3e: white solid. H NMR (3 MHz, CDCl 3 ) δ H :.87 (3H, t, J = 7, CH 3 alkyl),.9.44 (8H, m, 9(CH 2 ) alkyl),.47.7 (2H, m, CH 2 alkyl), 3.4 (3H, s, CH 3 ), 3.43 3.84 (7H, m), 4.2 (3H, br s, H), 4.74 (H, d, J = 4, CH-anomeric); 3 C NMR (75 MHz, CDCl 3 ) δ C : 4.25 (CH 3 alkyl), 22.82 (CH 2 alkyl), 26.7 (CH 2 alkyl), 2 (CH 2 alkyl), 29.67 (CH 2 alkyl), 29.73 (CH 2 alkyl), 29.77 (CH 2 alkyl), 29.8 (2CH 2 alkyl), 29.83 (CH 2 alkyl), 32.6 (CH 2 alkyl), 55.35 (CH 3 ), 7.33 (CH), (CH 2 ), 7.23 (CH), 72. (CH), 72.3 (CH 2 ), 74.49 (CH), 97 (CH-anomeric); IR ν max : 342 (H), 298 (-CH 3 ), 285 (-CH 2 -), 467, 37, 57, 5, 92; HRMS (ESI + ) calcd for C 9 H 38 Na 6 : 385.256 [M+Na] + ; found: 385.2558 (+.6 ppm); GC: R t = 26.4 min; Rf =.6 (: EtAc/EtH). 4e: white solid. H NMR (3 MHz, CDCl 3 ) δ H :.87 (3H, t, J = 7, CH 3 alkyl),.4.42 (8H, m, 9(CH 2 ) alkyl),.47.7 (2H, m, CH 2 alkyl), 2.6 7

(3H, br s, H), 3.24 (H, t, J = ); 3.4 (3H, s, CH 3 ), 3.49 (H, dd, J = = and 4), 4 3.66 (2H, m), 3.69 3.9 (4H, m), 4.74 (H, d, J = 4, CH-anomeric); 3 C NMR (75 MHz, CDCl 3 ) δ C : 4.26 (CH 3 alkyl), 22.83 (CH 2 alkyl), 26.2 (CH 2 alkyl), 29.49 (CH 2 alkyl), 29.64 (CH 2 alkyl), 29.74 (2CH 2 alkyl), 29.77 (CH 2 alkyl), 29.8 (CH 2 alkyl), 3.47 (CH 2 alkyl), 32.6 (CH 2 alkyl), 55.46 (CH 3 ), 6 (CH 2 ), 7.99 (CH), 72.8 (CH), 73.28 (CH 2 ), 7 (CH), 77.94 (CH), 99.2 (CH-anomeric); IR ν max : 3295 (H), 293 (-CH 3 ), 2848 (-CH 2 -), 739, 469, 37, 4, 67, 42, 993; C 9 H 38 Na 6 : 385.256 [M+Na] + ; found: 385.2574 (- ppm); GC: R t = 26.25 min.; Rf =.24 (: EtAc/EtH). 8

6. H and 3 C NMR spectra 6.. H and 3 C spectra of methyl -D-glucoside acetals 2a-e cg492-p Proton 4.736 4.723 38 2 5 4.6 4.88 3 3.479 3.43 3.36 3.38 3.263 3.232 2.87 2.786 E+8.97.99.99.99.92.4 2.94.95.. 2.3 4.4 3..657.64.628.364.357.34.328.323.36.37.898.875.85. 9. 8. 7. 6. 5. f (ppm) 4. 3. 2..5..5. H NMR (3 MHz, CDCl 3 ) Methyl 4,6--pentylidene -D-glucoside (2a) cg492-p 2.8 99.87 8.47 78 77.6 76.74 72.98 7.7 67 62.62 54 34.3 26.3 22.62 6E+8 6E+8 6E+8 5E+8 E+8-5 4 3 2 9 8 7 6 5 4 3 2 f (ppm) 3 C NMR (75 MHz, CDCl 3 ) Methyl 4,6--pentylidene -D-glucoside (2a) 9

cg49-p5 Proton 4.73 4.77 33 6 4.499 4. 4.83 4.67 3.833 3.82 74 67 6 8 3.474 3.397 3.258 3.226.627.63.65.373.349.268.258.245.88.859.836 E+8 E+8 E+8 8E+7 6E+7 4E+7 2E+7.97.96..3 2.3.22 2.99.33.87.99 2.3 3.88 3. -2E+7. 9. 8. 7. 6. 5. f (ppm) 4. 3. 2..5..5. H NMR (3 MHz, CDCl 3 ) Methyl 4,6--hexylidene -D-glucoside (2b) cg49-p5 2.8 99.9 8.49 78 77.6 76.74 72.95 7.6 66 62.62 5 34.28 3.74 23.86 22.62 4. 6E+8 6E+8 6E+8 5E+8 E+8-5 4 3 2 9 8 7 f (ppm) 6 5 4 3 2 3 C NMR (75 MHz, CDCl 3 ) Methyl 4,6--hexylidene -D-glucoside (2b)

cg488-p5 Proton 4.735 4.723 35 8 4.87 4.72 3.835 3.84 78 7 65 3.478 3.42 3.26 3.23.647.632.68.6.39.367.348.248.875.853.83 6E+8 5E+8 E+8.95.96.97.98 2.2.4 2.89.9.65 2.2 8.2 3. -. 9. 8. 7. 6. 5. f (ppm) 4. 3. 2..5..5. H NMR (3 MHz, CDCl 3 ) Methyl 4,6--octylidene -D-glucoside (2c) cg488-p5 2.82 99.88 8.48 78 77.6 76.74 72.97 7.68 66 62.62 53 34.33 3.85 2 29.26 24.8 22.73 4.8 9E+8 8E+8 7E+8 6E+8 5E+8 E+8 -E+8 5 4 3 2 9 8 7 f (ppm) 6 5 4 3 2 3 C NMR (75 MHz, CDCl 3 ) Methyl 4,6--octylidene -D-glucoside (2c)

RLCG38 4.754 4.74 49 32 5 3.84 3.89 88 75 58 45 27 3.494 3.42 3.276 3.245 2.68.67.66.645.63.624.45.38.36.25.889.868.845 6E+8 5E+8 E+8.94.93.96.97 2.6.2 2.75.98.8.93.87 3. -. 9. 8. 7. 6. 5. f (ppm) 4. 3. 2..5..5. H NMR (3 MHz, CDCl 3 ) Methyl 4,6--decylidene -D-glucoside (2d) RLCG38 RLCG38 R.Lafon CASYEN ML 8mg/CDCl3 2.64.2 3 78 77.6 76.73 72.65 7.9 68.43 64 55.2 34.9 3.82 29.49 29.46 29.25 24.8 29 4.3 5E+8 E+8-5 4 3 2 9 8 7 f (ppm) 6 5 4 3 2 3 C NMR (75 MHz, CDCl 3 ) Methyl 4,6--decylidene -D-glucoside (2d) 2

cg487-p5 Proton 4.745 4.732 4 24 8 3.838 84 7 4 9 3.486 3.4 3.269 3.238 2.853.663.653.638.624.67.69.597.396.372.352.239.885.863.84 E+8 E+8 E+8 8E+7 6E+7 4E+7 2E+7.9.92.93.94.93 2.7..78.9.95 5.69 3. -2E+7. 9. 8. 7. 6. 5. f (ppm) 4. 3. 2..5..5. H NMR (3 MHz, CDCl 3 ) Methyl 4,6--dodecylidene -D-glucoside (2e) cg487-p5 2.84 99.85 8.46 78 77.6 76.74 73.2 7.8 67 62.63 57 34.36 32.3 29.76 29.74 29.67 29.62 28 29.46 24.2 22.8 4.24 E+9 9E+8 8E+8 7E+8 6E+8 5E+8 E+8 -E+8 5 4 3 2 9 8 7 f (ppm) 6 5 4 3 2 3 C NMR (75 MHz, CDCl 3 ) Methyl 4,6--dodecylidene -D-glucoside (2e) 3

6.2. H and 3 C spectra of methyl -D-glucoside ethers 3a-e and 4a-e ChG59-P3 ChG59-P3 / CASYEN ML 4.77 4.696 4.682 3.7 3.62 9 3.499 3.465 3.457 3.442 3.434 3.42 3.4 3.43 3.365 3.344.57.547.524.52.28.269.257.245.233.865.843.82 6E+8 6E+8 6E+8 5E+8 E+8 3.9 7. 3.2 2. 3. -. 9. 8. 7. 6. 5. f (ppm) 4. 3. 2..5..5 H NMR (3 MHz, CDCl 3 ) Methyl 6--pentyl -D-glucoside (3a) ChG59-P3 ChG59-P3 / CASYEN ML 96 78 77.6 76.74 74.26 7 7.9 7.74 7 7.2 55.2 29.29 28.2 23 4.6 E+8 5 4 3 2 9 8 7 f (ppm) 6 5 4 3 2 3 C NMR (75 MHz, CDCl 3 ) Methyl 6--pentyl -D-glucoside (3a) 4

ChG59-P2 ChG59-P2 / CASYEN ML 4.72 4.7 3.88 3.8 3.79 3.778 3.744 3.734 68 44 37 3.389 3.37 3.22 3.8 8.558.536.54.299.287.276.264.254.882.86.838 E+8.92 6.99 2.95.4 9 2.4 4.7 3.. 9. 8. 7. 6. 5. f (ppm) 4. 3. 2..5..5. H NMR (3 MHz, CDCl 3 ) Methyl 4--pentyl -D-glucoside (4a) ChG59-P2 ChG59-P2 / CASYEN ML 99.35 77.86 78 77.6 76.74 72 73.4 72.6 7. 6.92 55.32 28.26 22.6 4. 8E+8 7E+8 6E+8 6E+8 6E+8 5E+8 E+8-4 3 2 9 8 7 f (ppm) 6 5 4 3 2 3 C NMR (75 MHz, CDCl 3 ) Methyl 4--pentyl -D-glucoside (4a) 5

ChG58-p4 ChG58-p4 / CASYEN ML 4.72 4.79 29 3.76 3.632 3.62 8 3.486 3.477 3.469 3.454 3.446 3.432 3.423 3.47 3.377 3.358 2.4.575.552.529.275.262.25.866.857.844.82 E+8 E+8 E+8 8E+7 6E+7 4E+7 2E+7.94 3.7 7.99 2.74 2.4 6.8 3. -2E+7. 9. 8. 7. 6. 5. f (ppm) 4. 3. 2..5..5. H NMR (3 MHz, CDCl 3 ) Methyl 6--hexyl -D-glucoside (3b) ChG58-p4 ChG58-p4 / CASYEN ML 98 78 77.36 77.6 76.74 74.28 72.3 7.94 7.79 5 7.24 55.8 5.47 3.75 29.6 29.49 25.75 22.66 4. E+8 5 4 3 2 9 8 7 f (ppm) 6 5 4 3 2 3 C NMR (75 MHz, CDCl 3 ) Methyl 6--hexyl -D-glucoside (3b) 6

ChG58-p2 ChG58-p2 / CASYEN ML 4.743 4.73 3.84 3.89 3.782 3.758 3.749 3.744 97 9 67 3.394 3.262 3.23 2.63 5E+8.577.554.529.57.36.338.38.276.242.89.885.869.846 E+8.92 3.9.95. 2.82.97 2.82 2.2 3.. 9. 8. 7. 6. 5. f (ppm) 4. 3. 2..5..5. H NMR (3 MHz, CDCl 3 ) Methyl 4--hexyl -D-glucoside (4b) ChG58-p2 ChG58-p2 / CASYEN ML 99.27 77.9 78 77.36 77.6 76.74 74.8 73.24 72.72 7. 6 55.4 3.8 3.38 25.83 22.72 4.6 5E+8 E+8-5 4 3 2 9 8 7 f (ppm) 6 5 4 3 2 3 C NMR (75 MHz, CDCl 3 ) Methyl 4--hexyl -D-glucoside (4b) 7

ChG499.6eth ChG499.6eth / Casyen ML 4.746 4.734 4.25 3.743 3.652 47 34 8 3.49 3.476 3.468 3.454 3.445 3.437 3.43 3.389.598.576.553.264.254.887.865.842 E+8 E+8 E+8 8E+7 6E+7 4E+7 2E+7.9 3.33 7 2.88.94 9.99 3. -2E+7. 9. 8. 7. 6. 5. f (ppm) 4. 3. 2..5..5. H NMR (3 MHz, CDCl 3 ) Methyl 6--octyl -D-glucoside (3c) ChG499.6eth ChG499.6eth / Casyen ML 99.6 78 77.36 77.6 76.74 74.44 72.24 72.8 7.2 7.44 55.3 3.96 29.72 29 29.39 2 22.78 4.22 5E+8 E+8-5 4 3 2 9 8 7 f (ppm) 6 5 4 3 2 3 C NMR (75 MHz, CDCl 3 ) Methyl 6--octyl -D-glucoside (3c) 8

ChG499.4eth ChG499.4eth / Casyen ML 7.379 4.743 4.73 3.87 3.8 3.78 3.758 3.748 95 89 7 64 3.394 3.26 3.23 8.576.553.53.269.252.885.863.84 E+8.95 3.8.98. 2.88.99 3. 2.8. 3.. 9. 8. 7. 6. 5. f (ppm) 4. 3. 2..5..5. H NMR (3 MHz, CDCl 3 ) Methyl 4--octyl -D-glucoside (4c) ChG499.4eth ChG499.4eth / Casyen ML 99.28 77.936 784 77.6 76.736 74.842 73.246 72.75 7.3 62.78 55.42 3.929 3.436 278 29.374 26.77 22.756 4.95 E+8 E+8 E+8 8E+7 6E+7 4E+7 2E+7-2E+7 5 4 3 2 9 8 7 f (ppm) 6 5 4 3 2 3 C NMR (75 MHz, CDCl 3 ) Methyl 4--octyl -D-glucoside (4c) 9

ChG478.6ethP ChG478.6ethP / CASYEN ML 4.74 4.727 4.38 3.734 3.72 3.679 3.646 38 25 6 3.493 3.484 3.469 3.462 3.444 3.438 3.43 3.396 3.382.59.57.548.24.27.883.862.838 E+8.84 3.38 7.83 2.6.98 3.73 3.. 9. 8. 7. 6. 5. f (ppm) 4. 3. 2..5..5. H NMR (3 MHz, CDCl 3 ) Methyl 6--decyl -D-glucoside (3d) ChG478.6ethP ChG478.6ethP / CASYEN ML 99.6 78 77.36 77.6 76.74 74.4 72.23 72.4 7.2 7.48 7.4 55.27 32.2 29.74 29.72 29.65 29.45 2 22.79 4.22 6E+8 5E+8 E+8-5 4 3 2 9 8 7 f (ppm) 6 5 4 3 2 3 C NMR(75 MHz, CDCl 3 ) Methyl 6--decyl -D-glucoside (3d) 2

cg355-rf Proton 4.76 4.748 3.837 3.827 3.88 3.84 3.783 3.776 3.762 3.752 3.66 85 5 2 3.437 3.4 3.247 2.7 2.32.592.568.545.256.897.876.853 E+8.89 3.23.89.9 2.69.8 3.86 2.8 2 2.92. 9. 8. 7. 6. 5. f (ppm) 4. 3. 2..5..5. H NMR (3 MHz, CDCl 3 ) Methyl 4--decyl -D-glucoside (4d) chg355.rf chg355.rf / CASYEN ML 99.93 77.953 784 77.364 77.6 76.737 75.82 73.287 72.87 7.99 62.77 55.473 32.32 3.467 29.734 29.75 29.632 29.455 26.26 22.823 4.257 E+8 E+8 9E+7 8E+7 7E+7 6E+7 4E+7 3E+7 2E+7 E+7 -E+7 4 3 2 9 8 7 f (ppm) 6 5 4 3 2 3 C NMR (75 MHz, CDCl 3 ) Methyl 4--decyl -D-glucoside (4d) 2

ChG49-4P ChG49-4P / CASYEN ML 4.75 4.738 4.2 3.654 4 3.492 3.48 3.47 3.459 3.447 3.439 3.47 3.394.578.555.246.892.87.847 6E+8 5E+8 E+8.7 3.24 6.89 2.72.9 7.4 3. -. 9. 8. 7. 6. 5. f (ppm) 4. 3. 2..5..5. H NMR (3 MHz, CDCl 3 ) Methyl 6--dodecyl -D-glucoside (3e) ChG49-4P ChG49-4P / CASYEN ML 973 784 77.363 77.6 76.737 74.487 72.294 72.97 7.23 7.333 55.354 36 29.828 29.796 29.777 29.73 29.67 29.498 26.7 22.82 4.248 5E+8 E+8 2 2 9 8 7 6 5 4 3 2 f (ppm) 9 8 7 6 5 4 3 2-3 C NMR (75 MHz, CDCl 3 ) Methyl 6--dodecyl -D-glucoside (3e) 22

ChG49-2P ChG49-2P / CASYEN ML 4.757 4.745 3.833 3.823 3.85 3.8 3.78 3.77 3.757 3.75 3.6 8 2 3.499 3.46 3.273 3.243 2.68.588.564.54.249.895.874.85 E+8.9 3.67.98.6 2.69.9 3.78.99 7.94 3.. 9. 8. 7. 6. 5. f (ppm) 4. 3. 2..5..5. H NMR (3 MHz, CDCl 3 ) Methyl 4--dodecyl -D-glucoside (4e) ChG49-2P ChG49-2P / CASYEN ML 99.2 77.94 78 77.36 77.6 76.74 7 73.28 72.8 7.99 6 55.46 32.6 3.47 29.8 29.77 29.74 29.64 29.49 26.2 22.83 4.26 E+8 E+8 E+8 8E+7 6E+7 4E+7 2E+7-2E+7 2 2 9 8 7 6 5 4 3 2 f (ppm) 9 8 7 6 5 4 3 2-3 C NMR (75 MHz, CDCl 3 ) Methyl 4--dodecyl -D-glucoside (4e) 23