Issue 3, 1998

Vinyltriphenylphosphonium Salt Mediated Serendipitous Synthesis of a Functionalized Pyrroloisoindole Derivative. New Synthesis of Trimethyl 5-Arylpyrrole-2,3,4-tricarboxylates

Abstract

N-Hydroxyphthalimide undergoes a complex reaction with dimethyl acetylenedicarboxylate in the presence of triphenylphosphine yielding a multiply functionalized pyrroloisoindole derivative which is then converted to trimethyl 5-arylpyrrole-2,3,4-tricarboxylate derivatives.

Article information

Article type
Paper

J. Chem. Res. (S), 1998, 166-167

Vinyltriphenylphosphonium Salt Mediated Serendipitous Synthesis of a Functionalized Pyrroloisoindole Derivative. New Synthesis of Trimethyl 5-Arylpyrrole-2,3,4-tricarboxylates

I. Yavari and M. Reza Islami, J. Chem. Res. (S), 1998, 166 DOI: 10.1039/A700719A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements