Title
The Application Of Vinylogous Iminium Salts And Related Synthons To The Regiocontrolled Preparation Of 2,3- And 2,5-Disubstituted Pyrroles
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.
Publication Date
5-13-1996
Publication Title
Tetrahedron
Volume
52
Issue
20
Number of Pages
6879-6892
Document Type
Article
Personal Identifier
scopus
DOI Link
https://doi.org/10.1016/0040-4020(96)00338-9
Copyright Status
Unknown
Socpus ID
0029873091 (Scopus)
Source API URL
https://api.elsevier.com/content/abstract/scopus_id/0029873091
STARS Citation
Gupton, John T.; Petrich, Scott A.; and Smith, Lana L., "The Application Of Vinylogous Iminium Salts And Related Synthons To The Regiocontrolled Preparation Of 2,3- And 2,5-Disubstituted Pyrroles" (1996). Scopus Export 1990s. 2498.
https://stars.library.ucf.edu/scopus1990/2498