A novel route to α-thiophenyl-γ-butyrolactones

Article abstract of DOI:10.1080/00397919208019284

An efficient, general route to α-thiophenyl-γ-butyrolactones using an aluminum thiophenoxide mediated Stobbe condensation is described.

Full text of DOI:10.1080/00397919208019284

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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A Novel Route to α-
Thiophenyl-γ-Butyrolactones
Jeremy I. Levin a
a American Cyanamid Company Medical Research
Division Lederle Laboratories , Pearl River, New
York, 10965
Published online: 24 Sep 2006.
To cite this article: Jeremy I. Levin (1992) A Novel Route to α-Thiophenyl-γ-
Butyrolactones, Synthetic Communications: An International Journal for
Rapid Communication of Synthetic Organic Chemistry, 22:7, 961-970, DOI:
10.1080/00397919208019284
To link to this article: http://dx.doi.org/10.1080/00397919208019284
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