2-Trialkylstannyl-5-tert-butoxyfurans: Convenient 5-substituted-2(3H)-furanone synthons

Article abstract of DOI:10.1080/00397919208021637

A versatile and mild route on 5-substituted-2(3H)-furanones (butenolides) from the palladium catalyzed coupling of aryl halides and 2-trialkylsannyl-5-tert-butoxyfurans is described.

Full text of DOI:10.1080/00397919208021637

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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2-Trialkylstannyl-5-tert-
butoxyfurans: Convenient 5-
Substituted-2(3H)-Furanone
Synthons
Bradley C. Pearce a
a Bristol-Myers Squibb Co., Pharmaceutical Research
Institute Wallingford , CT, 06492
Published online: 23 Sep 2006.
To cite this article: Bradley C. Pearce (1992) 2-Trialkylstannyl-5-tert-butoxyfurans:
Convenient 5-Substituted-2(3H)-Furanone Synthons, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry, 22:11,
1627-1643, DOI: 10.1080/00397919208021637
To link to this article: http://dx.doi.org/10.1080/00397919208021637
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