Ring-closing metathesis: A facile construct for alkaloid synthesis-Reference-Cited by-同舟云学术

Ring-closing metathesis: A facile construct for alkaloid synthesis

Published:2005-01-01 Issue:7 Volume:77 Page:1207-1212
ISSN:1365-3075
Container-title:Pure and Applied Chemistry
language:
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Author:

Martin Stephen F.¹

Affiliation:

1. 1Department of Chemistry and Biochemistry, The University of Texas, Austin, TX 78712, USA

Abstract

Ring-closing metathesis has been found to be a highly effective reaction for the synthesis of functionalized, bridged nitrogen heterocycles. The utility of the process has been established in several case studies, including a facile synthesis of the tropane ring system and efficient, enantioselective syntheses of the natural products (–)-peduncularine and (+)-anatoxin-a.

Publisher

Walter de Gruyter GmbH

Subject

General Chemical Engineering,General Chemistry

Link

https://www.degruyter.com/document/doi/10.1351/pac200577071207/pdf

Reference3 articles.

1. refs therein;Brenneman;Tetrahedron,2004

2. therein See also ) Handbook of New York a a For some examples see a See also refs For example see refs therein;Grubbs;Am Chem Soc Am Chem Soc Tetrahedron Lett Am Chem Soc Am Chem Soc Am Chem Soc Lett Org Chem,2003

3. a;Rigby;Synlett Tetrahedron Lett Am Chem Soc,1999

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