A Convenient Synthesis of Substituted Quinolines by Thermal Electrocyclic Rearrangement of o-Vinyl Anils under Nonacidic Conditions

DOI: 10.1021/jo00253a011

Source and publish data:

Journal of Organic Chemistry p. 4218 - 4222 (1988)

Update date:2022-08-04

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Authors:

Qiang, Lin Guo

Baine, Neil H.

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Article abstract of DOI:10.1021/jo00253a011

Anils 8a-g (Table II) underwent smooth rearrangement and oxidation to the quinolines 9a-g at 155-200 deg C via formation of the 2-3 carbon-carbon bond.These cyclizations proceeded in high yields under nonacidic conditions.It was often possible to prepare

Full text of DOI:10.1021/jo00253a011

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