中文名称 | 英文名称 | CAS号 | 化学式 | 分子量 |
---|---|---|---|---|
甲基2,3,4,6-四-O-(三甲基硅基)-Α-D-吡喃葡萄糖苷 | methyl 2,3,4,6-tetrakis-O-trimethylsilyl-α-D-glucopyranoside | 2641-79-4 | C19H46O6Si4 | 482.913 |
—— | Methyl 6-O-[(4-methylphenyl)sulfonyl]-2,3,4-tris-O-(trimethylsilyl)hexopyranoside | 180998-03-2 | C23H44O8SSi3 | 564.92 |
alpha-甲基葡萄糖甙 | methyl-alpha-D-glucopyranoside | 97-30-3 | C7H14O6 | 194.185 |
中文名称 | 英文名称 | CAS号 | 化学式 | 分子量 |
---|---|---|---|---|
—— | 2,3,4-tri-O-trimethylsilyl-1,6-anhydro-β-L-idopyranos-5-ulo-5-hydrate | 439614-70-7 | C15H34O6Si3 | 394.688 |
—— | [(2R,3R,4S,5R,6S)-2-(dichlorophosphoryloxymethyl)-6-methoxy-3,5-bis(trimethylsilyloxy)oxan-4-yl]oxy-trimethylsilane | 146399-90-8 | C16H37Cl2O7PSi3 | 527.602 |
—— | methyl 2,3,4-tri-O-trimethylsilyl-5-methylene-α-D-xylopyranoside | 6984-65-2 | C16H36O5Si3 | 392.715 |
—— | 5-O-tert-butyldimethylsilyl-1,6-anhydro-β-L-idopyranos-5-ulose | 316172-42-6 | C12H24O6Si | 292.404 |
—— | α-methyl-6-O-(dihydroxyphosphoryl)-D-glucopyranoside | 15416-98-5 | C7H15O9P | 274.164 |
—— | 2,3,4-tri-O-benzyl-5-O-tert-butyldimethylsilyl-1,6-anhydro-β-L-idopyranos-5-ulose | 316172-40-4 | C33H42O6Si | 562.778 |
—— | (3’S)-6-O-(3’,4’-dihydroxy-2’-methylenebutanoyl)-1-O-methyl-α-D-glucopyranoside | 1222854-44-5 | C12H20O9 | 308.285 |
Methyl α-D-glucopyranoside is converted to methyl 6-p-toluenesulfonyl-2,3,4-tris-O-trimethylsilyl- α-D-glucopyranoside 2 and then reacted with lithium diphenylphosphide in THF. When the reaction is carried out at room tem perature and below, S-O cleavage dominates giving methyl 2,3,4-tris-O-trimethylsilyl-α-D-glucopyranoside 3 , whereas at 60°C in THF or at 35°C in diethyl ether, C-O cleavage occurs yielding the title carbohydrate-phosphine 4 in good yield after deprotection