Journal Article

Functionalisation of 2-methoxy-6-methylpyridine

Synthetic Communications (1994) 24(10) 1367-1379
DOI: 10.1080/00397919408011740
23Citations
Citations of this article
8Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Selective bromination of 2-methoxy-6-methylpyridine 2 afforded 5-bromo-2-methoxy-6-methylpyridine 8. Deprotonation of this pyridine derivative in benzylic position or lithium-bromine exchange allowed the regio-selective introduction of various electrophiles. © 1994, Taylor & Francis Group, LLC. All rights reserved.

Cite

CITATION STYLE

APA

Gray, M. A., Konopski, L., & Langlois, Y. (1994). Functionalisation of 2-methoxy-6-methylpyridine. Synthetic Communications, 24(10), 1367–1379. https://doi.org/10.1080/00397919408011740

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free