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An Approach to the Synthesis of Tricholomalide A: An Effective Means for Achieving Homo-Robinson Annulation.

作者信息

Min Sun-Joon, Danishefsky Samuel J

机构信息

Department of Chemistry, Columbia University, 3000 Broadway, New York, NY 10027, USA.

出版信息

Tetrahedron Lett. 2008 May 19;49(21):3496-3499. doi: 10.1016/j.tetlet.2008.03.101.

Abstract

A procedure has been developed for the construction of 7,5-fused ring systems through ring expansion of silyl enol ethers. This method has been applied to the synthesis of an intermediate en route to the natural product, tricholomalide A.

摘要

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本文引用的文献

1
Total synthesis of guanacastepene a: a route to enantiomeric control.
J Org Chem. 2005 Dec 23;70(26):10619-37. doi: 10.1021/jo051470k.
2
Diterpenoids.
Nat Prod Rep. 2005 Oct;22(5):594-602. doi: 10.1039/b501834j. Epub 2005 Aug 19.
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Natural sesquiterpenoids.
Nat Prod Rep. 2005 Aug;22(4):465-86. doi: 10.1039/b501837b. Epub 2005 Jun 21.
4
Tricholomalides A-C, new neurotrophic diterpenes from the mushroom Tricholoma sp.
J Nat Prod. 2003 Dec;66(12):1578-81. doi: 10.1021/np030140x.

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