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Letter

Extending Pummerer Reaction Chemistry. Application to the Oxidative Cyclization of Tryptophan Derivatives

Supporting Info

Ken S. Feldman* and Andrew G. Karatjas

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

Org. Lett., 2004, 6 (17), pp 2849–2852

DOI: 10.1021/ol048974+

Publication Date (Web): July 30, 2004

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 β-oxygenated tryptophan derivative is reported. This process, which utilizes a new variant of the Pummerer reaction, may have application in TMC-95A synthesis.

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Published In Issue August 19, 2004
Received June 3, 2004

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Letter

Extending Pummerer Reaction Chemistry. Application to the Oxidative Cyclization of Tryptophan Derivatives

Abstract

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SciFinder Links

History

Recommend & Share

Related Content

A Short and Efficient Synthesis of (−)-7-Methylomuralide, a Potent Proteasome Inhibitor

Enantioselective Total Synthesis of (−)-Napyradiomycin A1 via Asymmetric Chlorination of an Isolated Olefin

Extending Pummerer Reaction Chemistry. Development of a Strategy for the Regio- and Stereoselective Oxidative Cyclization of 3-(ω-Nucleophile)-Tethered Indoles

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