庄治平, 周维善. 甾体不对称合成的研究Ⅶ.新法合成2-烷基-2-(3′-羰基-6′-甲氧基羰基)-己基-1,3-环戊二酮J. 药学学报, 1984, 19(9): 676-680.
引用本文: 庄治平, 周维善. 甾体不对称合成的研究Ⅶ.新法合成2-烷基-2-(3′-羰基-6′-甲氧基羰基)-己基-1,3-环戊二酮J. 药学学报, 1984, 19(9): 676-680.
ZHUANG Zhi-Ping, ZHOU Wei-Shan. STUDY ON ASYMMETRICAL SYNTHESIS OF STEROIDS.Ⅶ.A NOVEL METHOD FOR SYNTHESIS OF 2-ALKYL-2-(3'-OXO-6'-METHOXYCARBONYL-) HEXYL-1,3-CYCLOPENTANDIONEJ. Acta Pharmaceutica Sinica, 1984, 19(9): 676-680.
Citation: ZHUANG Zhi-Ping, ZHOU Wei-Shan. STUDY ON ASYMMETRICAL SYNTHESIS OF STEROIDS.Ⅶ.A NOVEL METHOD FOR SYNTHESIS OF 2-ALKYL-2-(3'-OXO-6'-METHOXYCARBONYL-) HEXYL-1,3-CYCLOPENTANDIONEJ. Acta Pharmaceutica Sinica, 1984, 19(9): 676-680.

甾体不对称合成的研究Ⅶ.新法合成2-烷基-2-(3′-羰基-6′-甲氧基羰基)-己基-1,3-环戊二酮

STUDY ON ASYMMETRICAL SYNTHESIS OF STEROIDS.Ⅶ.A NOVEL METHOD FOR SYNTHESIS OF 2-ALKYL-2-(3'-OXO-6'-METHOXYCARBONYL-) HEXYL-1,3-CYCLOPENTANDIONE

  • 摘要: 本文报道以丙烯醛为原料经γ-羰基亚砜合成了2-烷基-2-(3′-羰基-6′-甲氧基羰基)-己基-1,3-环戊二酮(2 a,b),7步总产率分别为13%和17%。2 a,b经微生物或S-氨基酸的不对称合成即得光学活性甾体药物全合成的合成原。

     

    Abstract: The 2-alkyl-2-(3′-oxo-6′-methoxycarbonyl-) hexyl-1, 3-cyclopentanedione(2) which can be converted to the optically active synthons by microbial asymmetric reduction or asymmetrical induction of S-amino acids is a key intermediate for total synthesis of steroids. Compound 2 was synthesized from acrolein (4) through the reaction sequence shown in scheme. The overall yields from 4 to 2 were 13% (R=CH3) and 17% (R=C2H5) respectively.

     

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