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Letter

Extending Pummerer Reaction Chemistry. Synthesis of (±)-Dibromophakellstatin by Oxidative Cyclization of an Imidazole Derivative

Supporting Info

Ken S. Feldman* and Amanda P. Skoumbourdis

Department of Chemistry, The Pennsylvania State University, University Park, Pennsylvania 16802

Org. Lett., 2005, 7 (5), pp 929–931

DOI: 10.1021/ol0500113

Publication Date (Web): February 5, 2005

In papers with more than one author, the asterisk indicates the name of the author to whom inquiries about the paper should be addressed.

, ksf@chem.psu.edu

Abstract

The diastereoselective oxidative cyclization of a dihydrooroidin derivative is reported. The thioimidate product formed by application of a new variant of the Pummerer reaction serves as a precursor to dibromophakellstatin.

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Published In Issue March 03, 2005
Received January 4, 2005

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Letter

Extending Pummerer Reaction Chemistry. Synthesis of (±)-Dibromophakellstatin by Oxidative Cyclization of an Imidazole Derivative

Abstract

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SciFinder Links

History

Recommend & Share

Related Content

Extending Pummerer Reaction Chemistry. Synthesis Studies in the Phakellin Alkaloid Area

Extending Pummerer Reaction Chemistry. Application to the Total Synthesis of (±)-Dibromoagelaspongin

Total Syntheses of (±)-Massadine and Massadine Chloride

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