Asymmetric Synthesis of the Carbon-14-Labeled Selective Glucocorticoid Receptor Modulator using Cinchona Alkaloid Catalyzed Addition of 6-Bromoindole to Ethyl Trifluoropyruvate

Asymmetric Synthesis of the Carbon-14-Labeled Selective Glucocorticoid Receptor Modulator using Cinchona Alkaloid Catalyzed Addition of 6-Bromoindole to Ethyl Trifluoropyruvate

We describe in this study the asymmetric synthesis of radioisotope (RI)-labeled selective glucocorticoid receptor modulator. This synthesis is based on optimization of the cinchona alkaloid catalyzed addition of 6-bromoindole to ethyl trifluoropyruvate and Negishi coupling of zinc cyanide to the 6-b...

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Bibliographic Details
Main Authors: Norie Tsuboya, Masanori Tobe, Tomoko Nakajima, Kazumi Niidome, Masato Sakamoto, Kengo Tojo, Daisuke Urabe, Takaaki Sumiyoshi
Format: Article
Language:English
Published: MDPI AG 2012-05-01
Series:Molecules
Subjects:
organocatalyst
cinchona alkaloid
asymmetric synthesis
radioisotope labeled compound
Online Access:http://www.mdpi.com/1420-3049/17/6/6507

Internet

http://www.mdpi.com/1420-3049/17/6/6507

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