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  4. Chiral Calcium Organophosphate-Catalyzed Enantioselective Electrophilic Amination of Enamides
 
research article

Chiral Calcium Organophosphate-Catalyzed Enantioselective Electrophilic Amination of Enamides

Drouet, Fleur
•
Lalli, Claudia
•
Liu, Hua
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2011
Organic Letters

Highly enantioselective direct amination of enamides catalyzed by chiral nonracemic calcium bis(phosphate) complex 3g afforded optically active 1,2-hydrazinoimines 4. Following a subsequent in situ hydrolysis or reduction, 2-hydrazinoketones 5 or syn-1,2-disubstituted 1,2- diamines 6 were obtained in high yields and excellent enantiomeric excess.

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Type
research article
DOI
10.1021/ol102625s
Web of Science ID

WOS:000285728000025

Author(s)
Drouet, Fleur
Lalli, Claudia
Liu, Hua
Masson, Geraldine
Zhu, Jieping  
Date Issued

2011

Publisher

American Chemical Society

Published in
Organic Letters
Volume

13

Issue

1

Start page

94

End page

97

Subjects

Asymmetric Alpha-Amination

•

Transition-Metal Catalysis

•

Bond-Forming Reactions

•

Bronsted Acid Catalysis

•

Stereoselective C-C

•

Ene-Type Reaction

•

Phosphoric-Acid

•

Reductive Amination

•

Carbonyl-Compounds

•

Amino-Acids

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LSPN  
Available on Infoscience
February 17, 2011
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/64466
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