Title

The Application Of Vinylogous Iminium Salts And Related Synthons To The Regiocontrolled Preparation Of 2,3- And 2,5-Disubstituted Pyrroles

Authors

Authors

J. T. Gupton; S. A. Petrich; L. L. Smith; M. A. Bruce; P. Vu; K. X. Du; E. E. Dueno; C. R. Jones;J. A. Sikorski

Comments

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Abbreviated Journal Title

Tetrahedron

Keywords

Chemistry, Organic

Abstract

The reaction of 1-substituted vinamidinium salts with sarcosine ethyl ester produced 2,3-disubstituted pyrroles; a similar reaction with glycine ethyl ester gave 2,5-disubstituted pyrroles. Reactions of related three-carbon synthons with sarcosine and glycine were studied under basic, neutral and acidic conditions which demonstrated the utility of these derivatives for the regiocontrolled preparation of disubstituted pyrroles. Copyright (C) 1996 Elsevier Science Ltd

Journal Title

Tetrahedron

Volume

52

Issue/Number

20

Publication Date

1-1-1996

Document Type

Article

DOI Link

http://dx.doi.org/10.1016/0040-4020(96)00338-9

Language

English

First Page

6879

Last Page

6892

WOS Identifier

WOS:A1996UK08900004

ISSN

0040-4020

Recommended Citation

"The Application Of Vinylogous Iminium Salts And Related Synthons To The Regiocontrolled Preparation Of 2,3- And 2,5-Disubstituted Pyrroles" (1996). Faculty Bibliography 1990s. 3040.
https://stars.library.ucf.edu/facultybib1990/3040