Liebigs Annalen Der Chemie

Chemie der Ginkgolide, IV. Herstellung von Ginkgolid B aus Ginkgolid C

K Weinges, H Schick

Index: Weinges, Klaus; Schick, Hartmut Liebigs Annalen der Chemie, 1991 , # 1 p. 81 - 83

Full Text: HTML

Citation Number: 15

Abstract

The reaction of ginkgolide C (3) with tert-butylchlorodiphenylsilane results exclusively in the formation of the 1-0-tertbutyldiphenylsilyl ether 5, which when treated with 0- phenylchlorothioformate leads to the 7-phenyloxythiocarbonyl derivative 6. The reduction of 6 with tributyltin hydride/AIBN yields the 1-0-tert-butyldiphenylsilyl ether 7 of ginkgolide B (2). Removal of the silyl protective group with tetrabutylammonium fluoride gives pure ...

Related Articles:

Intramolecular and intermolecular hydroxyl reactivity differences in ginkgolides A, B and C and their chemical applications

[Tetrahedron Letters, , vol. 33, # 46 p. 6955 - 6958]

Intramolecular and intermolecular hydroxyl reactivity differences in ginkgolides A, B and C and their chemical applications

[Tetrahedron Letters, , vol. 33, # 46 p. 6955 - 6958]

Intramolecular and intermolecular hydroxyl reactivity differences in ginkgolides A, B and C and their chemical applications

[Tetrahedron Letters, , vol. 33, # 46 p. 6955 - 6958]

Intramolecular and intermolecular hydroxyl reactivity differences in ginkgolides A, B and C and their chemical applications

[Tetrahedron Letters, , vol. 33, # 46 p. 6955 - 6958]

Preparation of a tritiated ginkgolide

[Bioorganic and Medicinal Chemistry Letters, , vol. 14, # 22 p. 5673 - 5675]

More Articles...