Activation of macrocyclic enediynes by transannular cyclization

Basak, Amit ; Roy, Sandip Kumar ; Mandal, Subrata (2004) Activation of macrocyclic enediynes by transannular cyclization Angewandte Chemie International Edition, 44 (1). pp. 132-135. ISSN 1433-7851

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Official URL: http://www3.interscience.wiley.com/journal/1098582...

Related URL: http://dx.doi.org/10.1002/ange.200460831

Abstract

Two N-protected macrocyclic enediynes have been synthesized by intramolecular N-alkylation. The smaller 12-membered enediyne, upon deprotection, yields a stable amine. In contrast, the amine generated from the 13-membered enediyne forms the aminol, which in turn undergoes a spontaneous Bergman cyclization.

Item Type:Article
Source:Copyright of this article belongs to John Wiley and Sons, Inc.
Keywords:Cyclization; DNA Damage; Enediynes; Macrocycles
ID Code:1676
Deposited On:05 Oct 2010 09:51
Last Modified:13 Jan 2011 10:12

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