New entry to chiral butenolide synthons. Application to expeditious syntheses of (+)-nephrosteranic acid, (+)-trans-whisky lactone, and (+)-trans-cognac lactone-Reference-Cited by-同舟云学术

New entry to chiral butenolide synthons. Application to expeditious syntheses of (+)-nephrosteranic acid, (+)-trans-whisky lactone, and (+)-trans-cognac lactone

Published:1994-06 Issue:24 Volume:35 Page:4123-4124
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Takahata Hiroki,Uchida Yasuhiro,Momose Takefumi

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference15 articles.

1. Reflections on the total synthesis of natural products: Art, craft, logic, and the chiron approach

2. New general asymmetric synthesis of versatile .gamma.-alkylated butenolides and its application to expeditious synthesis of the chiral Geissman-Waiss lactones useful for (+)-retronecine synthesis

3. Highly Selective Intramolecular Heterocyclization and Its Application to Synthesis of Biologically Active Compounds

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