Tandem Addition/Cyclization of Alkynylzinc Reagents to Enantiopure 2-tert-Butyl-3,5-dimethyl-2,3-dihydroimidazol-4-oneN-Oxide: Potential Precursors of Quaternary α-Amino Acids-Reference-Cited by-同舟云学术

Tandem Addition/Cyclization of Alkynylzinc Reagents to Enantiopure 2-tert-Butyl-3,5-dimethyl-2,3-dihydroimidazol-4-oneN-Oxide: Potential Precursors of Quaternary α-Amino Acids

Published:2005-07 Issue:13 Volume:2005 Page:2694-2701
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Cantagrel Frédéric,Pinet Sandra,Gimbert Yves,Chavant Pierre Y.

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference56 articles.

1. N-hydroxy .alpha.-amino acids in organic chemistry

2. Selenium dioxide catalyzed oxidation of secondary amines with hydrogen peroxide. Simple synthesis of nitrones from secondary amines

3. Tungstate-catalyzed oxidation of secondary amines to nitrones. .alpha.-Substitution of secondary amines via nitrones

4. Oxidation of secondary amines to nitrones using urea-hydrogen peroxide complex (UHP) and metal catalysts

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