Mild generation of o-quinodimethanes via fluoride induced 1,4-elimination of α-(o-trimethylsilylmethyl)benzylesters: stereoselective synthesis of 19-nor steroids and RU486 precursors-Reference-Cited by-同舟云学术

Mild generation of o-quinodimethanes via fluoride induced 1,4-elimination of α-(o-trimethylsilylmethyl)benzylesters: stereoselective synthesis of 19-nor steroids and RU486 precursors

Published:2006-07 Issue:27 Volume:47 Page:4671-4675
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Port Marc,Lett Robert

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference33 articles.

1. A formal regio- and stereoselective total synthesis of estrone. A convenient synthesis of D-homoestrone

2. Recent advances in the total synthesis of steroids via intramolecular cycloaddition reactions

3. Second generation of steroid synthesis via o-quinodimethane

4. Intramolecular Cycloaddition Reactions ofortho-Quinodimethanes in Organic Synthesis

5. Preparation and Use of Nitrogen- or Sulphurcontaining Heterocycles in Organic Synthesis

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