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  4. Phosphoric Acid Catalyzed Diastereo- and Enantioselective Synthesis of Substituted 1,3-Diaminotetralins
 
research article

Phosphoric Acid Catalyzed Diastereo- and Enantioselective Synthesis of Substituted 1,3-Diaminotetralins

Dagousset, Guillaume
•
Erb, William
•
Zhu, Jieping  
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2014
Organic Letters

The reaction of anilines and phenylacetaldehydes in the presence of chiral phosphoric acid afforded optically active 1,2-trans, 2,3-cis 1,3-diaminotetralins in high yields with excellent diastereo- and enantioselectivities. The trans/cis product was readily isomerized to a trans/trans stereoisomer with no significant loss of enantiomeric purity.

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Type
research article
DOI
10.1021/ol500946w
Web of Science ID

WOS:000335491000065

Author(s)
Dagousset, Guillaume
Erb, William
Zhu, Jieping  
Masson, Géraldine
Date Issued

2014

Publisher

Amer Chemical Soc

Published in
Organic Letters
Volume

16

Issue

9

Start page

2554

End page

2557

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LSPN  
Available on Infoscience
May 14, 2014
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/103301
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