Issue 16, 1997
From the journal:

Chemical Communications

3,4-Bis(trimethylsilyl)-1H-pyrrole: a versatile building block for unsymmetrically 3,4-disubstituted pyrroles

Ho-Wai Chan,   Po-Ching Chan,   Jian-Hui Liu  and  Henry N. C. Wong  

Abstract

3,4-Bis(trimethylsilyl)-1H-pyrrole 1c functions as a versatile building block for the construction of unsymmetrically 3,4-disubstituted pyrroles through the use of stepwise regiospecific ipso mono-halogenation, Sonogashira cross-coupling reactions and Suzuki cross-coupling reactions; the advantages of this strategy lie in its stepwise manner as well as in its prospect of yielding 3,4-disubstituted pyrroles with diverse substitution patterns.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/A703921B
Article type
Paper

Chem. Commun., 1997, 1515-1516

Permissions

Request permissions

3,4-Bis(trimethylsilyl)-1H-pyrrole: a versatile building block for unsymmetrically 3,4-disubstituted pyrroles

H. Chan, P. Chan, J. Liu and H. N. C. Wong, Chem. Commun., 1997, 1515 DOI: 10.1039/A703921B

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.

Social activity

Spotlight

Advertisements