The Baylis–Hillman approach to quinoline derivatives

Title: The Baylis–Hillman approach to quinoline derivatives
Creator: Familoni, Oluwole B, Klaas, Phindile J, Lobb, Kevin A, Pakade, Vusumzi E, Kaye, Perry T
Subject: To be catalogued
Date: 2006
Type: text
Type: article
Identifier: http://hdl.handle.net/10962/479070
Identifier: vital:78258
Identifier: https://pubs.rsc.org/en/content/articlelanding/2006/ob/b608592j/unauth
Description: Baylis–Hillman reactions of 2-nitrobenzaldehydes with various activated alkenes afford adducts that undergo reductive cyclisation to quinoline derivatives. The chemo- and regioselectivity of cyclisation appears to be influenced by the choice of both the substrate and the reagent system, and competing reactions have been observed.
Format: 6 pages, pdf
Language: English
Relation: Organic and Biomolecular Chemistry, Familoni, O.B., Klaas, P.J., Lobb, K.A., Pakade, V.E. and Kaye, P.T., 2006. The Baylis–Hillman approach to quinoline derivatives. Organic and Biomolecular Chemistry, 4(21), pp.3960-3965, Organic and Biomolecular Chemistry volume 4 number 21 3960 3965 2006 1477-0539
Rights: Publisher
Rights: Use of this resource is governed by the terms and conditions of the Royal Society of Chemistry Terms and Conditions Statement (https://0-www.rsc.org.wam.seals.ac.za/help-legal/)

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Kaye, Perry T (Distinguished Fellow Emeritus Professor)

Lobb, Kevin Allan (Assoc Prof)

RU Department of Chemistry

SDG 03. Good Health and Well-Being

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