Chromone Studies. Part 17. Tricyclic Scaffolds from Reactions of chromone-3-carbaldehydes and methyl vinyl ketone under Baylis–Hillman conditions

Ganto, Mlungiseleli M; Molefe, Duduzile M; Lobb, Kevin A; Kaye, Perry T

Title: Chromone Studies. Part 17. Tricyclic Scaffolds from Reactions of chromone-3-carbaldehydes and methyl vinyl ketone under Baylis–Hillman conditions
Creator: Ganto, Mlungiseleli M
Creator: Molefe, Duduzile M
Creator: Lobb, Kevin A
Creator: Kaye, Perry T
Subject: To be catalogued
Date Issued: 2009
Date: 2009
Type: text
Type: article
Identifier: http://hdl.handle.net/10962/449321
Identifier: vital:74811
Identifier: xlink:href="https://doi.org/10.3184/030823409X4652"
Description: Reaction of a series of chromone-3-carbaldehydes with methyl vinyl ketone under Baylis–Hillman conditions, using 3-hydroxyquinuclidine in chloroform or DABCO in 1-methyl-2-pyrrolidinone, affords unprecedented tricylic chromone derivatives which, depending on the conditions, may be accompanied by the normal Baylis–Hillman products or their respective tricyclic dimers.
Format: computer
Format: online resource
Format: application/pdf
Format: 1 online resource (5 pages)
Format: pdf
Publisher: SAGE
Language: English
Relation: Journal of Chemical Research
Relation: Molefe, D.M., Ganto, M.M., Lobb, K.A. and Kaye, P.T., 2009. Chromone Studies. Part 17. Tricyclic Scaffolds from Reactions of chromone-3-carbaldehydes and methyl vinyl ketone under Baylis–Hillman conditions. Journal of Chemical Research, 2009(7), pp.452-456
Relation: Journal of Chemical Research volume 2009 number 7 p. 452 2009 2047-6507
Rights: Publisher
Rights: Use of this resource is governed by the terms and conditions of the Sage Journals Terms and Conditions Statement (https://journals.sagepub.com/page/policies/terms-of-use)
Rights: Open Access

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RU Centre for Chemico- and Biomedicinal Research (CCBR)

Kaye, Perry T (Distinguished Fellow Emeritus Professor)

Lobb, Kevin Allan (Assoc Prof)

SDG 03. Good Health and Well-Being

RU Department of Chemistry

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