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【结 构 式】

【分子编号】29882

【品名】[[1-(benzyloxy)vinyl]oxy](trimethyl)silane; benzyl 1-[(trimethylsilyl)oxy]vinyl ether

【CA登记号】

【 分 子 式 】C12H18O2Si

【 分 子 量 】222.35922

【元素组成】C 64.82% H 8.16% O 14.39% Si 12.63%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:

(ii) The asymmetric construction of the hydroxymercaptoheptenoic acid: For construction of the hydroxymercaptoheptenoic acid (VIII), cesium triphenylmethylthiolate anion was added to methyl 2,4-pentadienoate (V), which resulted in a beta,gamma-unsaturated methyl ester that was converted to an alpha,beta-unsaturated ester after exposure to Cs2CO3. DIBAL reduction to the primary alcohol followed by Swern oxidation yielded the alpha,beta-unsaturated aldehyde (VI). In the presence of the ligand derived from (R)-(-)-binaphthyl amino alcohol, Ti(IV)-catalyzed addition of O-benzyl, O-TMS ketene acetal to the alpha,beta-unsaturated aldehyde (VI) resulted in the aldol product (VII). Hydrolysis of the benzyl ester with LiOH in aqueous methanol formed the beta-hydroxymercaptoheptenoic acid (VIII).

1 Li, K.W.; Simon, J.A.; Xing, W.; Wu, J.; Total synthesis of the antitumor depsipeptide FR901228. J Am Chem Soc 1996, 118, 30, 7237.
2 Wang, H.-C. R.; FR901228. Drugs Fut 1999, 24, 11, 1184.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
29882 [[1-(benzyloxy)vinyl]oxy](trimethyl)silane; benzyl 1-[(trimethylsilyl)oxy]vinyl ether C12H18O2Si 详情 详情
(V) 29880 methyl (2E)-2,4-pentadienoate C6H8O2 详情 详情
(VI) 29881 (E)-5-(tritylsulfanyl)-2-pentenoic acid C24H22O2S 详情 详情
(VII) 29883 benzyl (3R,4E)-3-hydroxy-7-(tritylsulfanyl)-4-heptenoate C33H32O3S 详情 详情
(VIII) 29884 (3R,4E)-3-hydroxy-7-(tritylsulfanyl)-4-heptenoic acid C26H26O3S 详情 详情
Extended Information