Studies for the synthesis of marine natural products-Reference-Cited by-同舟云学术

Studies for the synthesis of marine natural products

Published:2009-01-01 Issue:2 Volume:81 Page:181-194
ISSN:1365-3075
Container-title:Pure and Applied Chemistry
language:
Short-container-title:

Author:

Williams David R.¹,Walsh Martin J.¹,Claeboe Christopher D.¹,Zorn Nicolas¹

Affiliation:

1. 1Department of Chemistry, Indiana University, 800 East Kirkwood Avenue, Bloomington, IN 47405-7102, USA

Abstract

The process of allylic transposition in SE' reactions is a significant construct for synthesis. The flexibility of a variety of allylation strategies provides for the rational design of pathways to a diverse array of complex targets. Our recent studies of SE' reactions will examine issues of stereoselectivity and efficiency in the context of applications toward the synthesis of marine natural products such as the xenicane diterpenes, which feature the strained E-cyclononene ring system, and peloruside A, a 16-membered macrocyclic lactone.

Publisher

Walter de Gruyter GmbH

Subject

General Chemical Engineering,General Chemistry

Link

https://www.degruyter.com/downloadpdf/journals/pac/81/2/article-p181.xml

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