Issue 15, 2002

Heteroaryl radicals. Part 1. Synthesis of linear pyridine-fused ring systems by endo-selective 2-pyridyl radical cyclizations

Abstract

Bu3SnH-induced 2-pyridyl radicals, derived from the 2-bromopyridinyl-substituted methylenecyclohexane 4 and also the vinyl- and the allyl-cyclohexanols 5 and 6, undergo endo-selective cyclizations to give six-, seven- and eight-membered-ring annulated pyridines 7, 11 and 12.

Graphical abstract: Heteroaryl radicals. Part 1. Synthesis of linear pyridine-fused ring systems by endo-selective 2-pyridyl radical cyclizations

Article information

Article type
Paper
Submitted
08 May 2002
Accepted
11 Jun 2002
First published
26 Jun 2002

J. Chem. Soc., Perkin Trans. 1, 2002, 1769-1773

Heteroaryl radicals. Part 1. Synthesis of linear pyridine-fused ring systems by endo-selective 2-pyridyl radical cyclizations

S. Maiti, B. Achari, R. Mukhopadhyay and A. Kr. Banerjee, J. Chem. Soc., Perkin Trans. 1, 2002, 1769 DOI: 10.1039/B204436F

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