V. V. Vashchenko, V. V. Kravets, L. A. Kutulya, “Bromination of 2-Arylideneketones”, Mendeleev Commun., 5:4 (1995), 159

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Mendeleev Communications, 1995, Volume 5, Issue 4, Pages 159–160
DOI: https://doi.org/10.1070/MC1995v005n04ABEH000506 (Mi mendc5080)

This article is cited in 1 scientific paper (total in 1 paper)

Bromination of 2-Arylideneketones

V. V. Vashchenko, V. V. Kravets, L. A. Kutulya

STC 'Institute for Single Crystals', National Academy of Sciences of Ukraine, Kharkov, Ukraine

Full-text PDF (196 kB) Citations (1)

DOI: https://doi.org/10.1070/MC1995v005n04ABEH000506

Abstract: It is shown that the acid catalysed bromination of α,β-unsaturated ketones by NBS occurs in the α’-position in high yield; this reaction with chiral (1R,4R)-2-arylidene-p-menthanones is diastereoselective and results in 1R,4S-diastereoisomers.

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Document Type: Article

Language: English

Citation: V. V. Vashchenko, V. V. Kravets, L. A. Kutulya, “Bromination of 2-Arylideneketones”, Mendeleev Commun., 5:4 (1995), 159–160

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This publication is cited in the following 1 articles:

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