Tunable Regioselectivity Associated with the Reaction of 2,3-Dihalo-1-(phenylsulfonyl)-1-propenes with Ambident Nucleophilic Reagents

DOI: 10.1021/jo00030a024

Source and publish data:

Journal of Organic Chemistry p. 1161 - 1169 (1992)

Update date:2022-07-30

Topics: Regioselectivity Reaction Experiment Ambident Tunable Nucleophilic reagents

Authors:

Padwa, Albert

Austin, David J.

Ishida, Masaru

Muller, Cheryl L.

Murphree, S. Shaun

Yeske, Philip E.

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Article abstract of DOI:10.1021/jo00030a024

2,3-Dihalo-1-(phenylsulfonyl)-1-propenes, obtained by the addition of bromine or iodine onto (phenylsulfonyl)propadiene, were found to exhibit interesting reactivity as both mono- and dielectrophiles, with the mode of reactivity depending upon the nature

Full text of DOI:10.1021/jo00030a024

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Product name:Benzene, [(3-bromo-2-methoxy-1-propenyl)sulfonyl]-, (Z)-

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