中文名称 | 英文名称 | CAS号 | 化学式 | 分子量 |
---|---|---|---|---|
(2S)-3-[[(叔丁基)二甲基硅烷基]氧基]-2-甲基-1-丙醇 | (S)-3-(tert-butyldimethylsilyloxy)-2-methylpropan-1-ol | 105859-45-8 | C10H24O2Si | 204.385 |
(2R)-3-[[(叔丁基)二甲基硅烷基]氧基]-2-甲基丙酸甲酯 | methyl (R)-2-methyl-3-[(tert-butyldimethylsilyl)oxy]propionate | 105859-44-7 | C11H24O3Si | 232.395 |
中文名称 | 英文名称 | CAS号 | 化学式 | 分子量 |
---|---|---|---|---|
—— | (2R,4S,5R,6S)-1-([tert-butyldimethylsilyl]oxy)-5-hydroxy-2,4,6,8-tetramethyl-8-nonen-3-one | 464928-35-6 | C19H38O3Si | 342.594 |
The asymmetric synthesis of the C15C23unit of Leptomycin B (LMB) is described. All four stereocenters of the C15C23unit were prepared from one building block exhibiting only one stereocenter. This building block was synthesized via either an enzymatic transformation or starting from a chiral reagent.Key words: Leptomycin, natural product synthesis, enzymatic transformation, Aldol reaction, Pseudomonas fluorescence lipase (PFL).