The synthesis of butenolide a-formyl acetals

C. Chen; K. Kejian; A. Mark; S. Sanner; Robert M Carlson

doi:10.1080/00397919008052338

The synthesis of butenolide a-formyl acetals

C. Chen, K. Kejian, A. Mark, S. Sanner, Robert M Carlson

Chemistry & Biochemistry

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5 Scopus citations

Abstract

The dianion generated from 3-phenylthio-2-phenylthio-methylpropenoic acid adds to a series of carbonyl compounds to give, after methanolysis, a-dimethoxymethyl-a-butenolides.

Original language	English (US)
Pages (from-to)	901-906
Number of pages	6
Journal	Synthetic Communications
Volume	20
Issue number	6
DOIs	https://doi.org/10.1080/00397919008052338
State	Published - Jan 1 1990

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title = "The synthesis of butenolide a-formyl acetals",

abstract = "The dianion generated from 3-phenylthio-2-phenylthio-methylpropenoic acid adds to a series of carbonyl compounds to give, after methanolysis, a-dimethoxymethyl-a-butenolides.",

author = "C. Chen and K. Kejian and A. Mark and S. Sanner and Carlson, {Robert M}",

year = "1990",

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doi = "10.1080/00397919008052338",

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journal = "Synthetic Communications",

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T1 - The synthesis of butenolide a-formyl acetals

AU - Chen, C.

AU - Kejian, K.

AU - Mark, A.

AU - Sanner, S.

AU - Carlson, Robert M

PY - 1990/1/1

Y1 - 1990/1/1

N2 - The dianion generated from 3-phenylthio-2-phenylthio-methylpropenoic acid adds to a series of carbonyl compounds to give, after methanolysis, a-dimethoxymethyl-a-butenolides.

AB - The dianion generated from 3-phenylthio-2-phenylthio-methylpropenoic acid adds to a series of carbonyl compounds to give, after methanolysis, a-dimethoxymethyl-a-butenolides.

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U2 - 10.1080/00397919008052338

DO - 10.1080/00397919008052338

M3 - Article

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VL - 20

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EP - 906

JO - Synthetic Communications

JF - Synthetic Communications

IS - 6

ER -

The synthesis of butenolide a-formyl acetals

Abstract

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