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  4. Palladium catalyzed reductive deprotection of alloc: Transprotection and peptide bond formation
 
research article

Palladium catalyzed reductive deprotection of alloc: Transprotection and peptide bond formation

Beugelmans, René
•
Neuville, Luc
•
Bois-Choussy, Michèle
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1995
Tetrahedron Letters

N-allyloxycarbonyl group could be efficiently removed using sodium borohydride as hydride donor in the presence of catalytic amount of palladium (0). The conditions were applied to chemoselective protecting group transformation (transprotection) and peptide bond formation.

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Type
research article
DOI
10.1016/0040-4039(95)00449-M
Author(s)
Beugelmans, René
•
Neuville, Luc
•
Bois-Choussy, Michèle
•
Chastanet, Jacqueline
•
Zhu, Jieping  
Date Issued

1995

Publisher

Elsevier

Published in
Tetrahedron Letters
Volume

36

Issue

18

Start page

3129

End page

3132

Editorial or Peer reviewed

REVIEWED

Written at

OTHER

EPFL units
LSPN  
Available on Infoscience
November 25, 2010
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/58707
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