Tricyclic isoindolines by Heck cyclization

G, Satyanarayana and Maier, M E (2012) Tricyclic isoindolines by Heck cyclization. Tetrahedron, 68 (6). pp. 1745-1749. ISSN 0040-4020

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Abstract

A series of 4-formyl esters 8a-d was prepared by Michael addition of an enamine with ethyl acrylate. A subsequent condensation with 2-bromobenzylamines 3 gave rise to cyclic enamides 9aa-dd. In a Heck cyclization reaction tricyclic isoindoles 10aa-dd were formed in good yields. © 2011 Elsevier Ltd. All rights reserved.

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IITH Creators:	IITH Creators ORCiD G, Satyanarayana UNSPECIFIED
Item Type:	Article
Uncontrolled Keywords:	Enamides; Heck cyclization; Heterocycles; Isoindoles; Pyridones;
Subjects:	?? sub5.8 ??
Divisions:	Department of Chemistry
Depositing User:	Users 3 not found.
Date Deposited:	14 Oct 2014 09:37
Last Modified:	24 Sep 2015 10:26
URI:	http://raiithold.iith.ac.in/id/eprint/462
Publisher URL:	http://dx.doi.org/10.1016/j.tet.2011.12.060
OA policy:	http://www.sherpa.ac.uk/romeo/issn/0040-4020/
Related URLs:	Google Scholar

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