The application of vinylogous iminium salts and related synthons to the regiocontrolled preparation of 2,3- and 2,5-disubstituted pyrroles

DOI: 10.1016/0040-4020(96)00338-9

Source and publish data:

Tetrahedron p. 6879 - 6892 (1996)

Update date:2022-07-30

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Authors:

Gupton, John T.

Petrich, Scott A.

Smith, Lana L.

Bruce, Marc A.

Vu, Phong

Du, Karen X.

Dueno, Eric E.

Jones, Claude R.

Sikorski, James A.

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Article abstract of DOI:10.1016/0040-4020(96)00338-9

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 gly

Full text of DOI:10.1016/0040-4020(96)00338-9

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