A short synthesis of γ-lactams via the spontaneous ring expansion of β-lactams

Article abstract of DOI:10.1080/00397919208021675

β-Lactams, derived via the cycloaddition of chlorosulfonyl isocyanate to alkenes, undergo thermal rearrangement at room temperature to affort γ-lactams.

Full text of DOI:10.1080/00397919208021675

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Synthetic Communications: An
International Journal for Rapid
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Organic Chemistry
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A Short Synthesis of γ-Lactams
Via the Spontaneous Ring
Expansion of β-Lactams
T. Howard Black a , John T. Olson a & Daniel C. Abt a
a Department of Chemistry , Eastern Illinois
University Charleston , Illinois, 61920
Published online: 23 Sep 2006.
To cite this article: T. Howard Black , John T. Olson & Daniel C. Abt (1992) A Short
Synthesis of γ-Lactams Via the Spontaneous Ring Expansion of β-Lactams, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 22:18, 2729-2733, DOI: 10.1080/00397919208021675
To link to this article: http://dx.doi.org/10.1080/00397919208021675
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