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Communication

Catalytic Enantioselective Conjugate Addition of Carbamates

Supporting Info

Claudio Palomo,* Mikel Oiarbide, Rajkumar Halder, Michael Kelso, Enrique Gómez-Bengoa, and Jesús M. García^†

Departamento de Qumica Orgnica I, Facultad de Qumica, Universidad del Pas Vasco, Apdo. 1072, 20080 San Sebastin, Spain

J. Am. Chem. Soc., 2004, 126 (30), pp 9188–9189

DOI: 10.1021/ja047004e

Publication Date (Web): July 9, 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.

†

Current address: Departamento de Química Aplicada, Universidad Pública de Navarra, Campus de Arrosadía, 31006 Pamplona, Spain.

, qoppanic@sc.ehu.es

Abstract

Catalytic, asymmetric conjugate addition of carbamates to enoyl systems has been realized for the first time, providing a two-step access to virtually enantiopure N-protected β-amino acids.

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Published In Issue August 04, 2004
Received May 21, 2004

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Communication

Catalytic Enantioselective Conjugate Addition of Carbamates

Abstract

Tools

SciFinder Links

History

Recommend & Share

Related Content

Stereoselective Construction of Seven-Membered Rings with an All-Carbon Quaternary Center by Direct Tiffeneau−Demjanov-type Ring Expansion

Highly Enantioselective Friedel−Crafts Alkylations of Pyrroles and Indoles with α‘-Hydroxy Enones under Cu(II)-Simple Bis(oxazoline) Catalysis

Enantiospecific Total Syntheses of Kapakahines B and F

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