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  4. Highly Stereoselective Synthesis of (+/-)-Aminobromocyclitol Derivatives from Furan
 
research article

Highly Stereoselective Synthesis of (+/-)-Aminobromocyclitol Derivatives from Furan

Reynard, E.
•
Reymond, J. L.
•
Vogel, P.  
1991
Synlett

The Diels-Alder adduct (2-cyano-7-oxabicyclo[2.2.1]-hept-5-en-2-yl acetate) of furan and 1-cyanovinyl acetate was converted to N-[(1RS,2RS,3RS,4SR,6RS)-2,3,4-triacetoxy-6-bromocyclohex-1-yl]benzamide and to N-[(1RS,2RS,3SR,4RS,5SR,6SR)-2,3,4,5-tetraacetoxy-6-bromocyclohex-1-yl]b enzamide with high stereoselectivity.

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Type
research article
DOI
10.1055/s-1991-20763
Author(s)
Reynard, E.
Reymond, J. L.
Vogel, P.  
Date Issued

1991

Published in
Synlett
Issue

7

Start page

469

End page

471

Subjects

Diels-alder reaction

•

pseudo-sugars

•

naked sugars

•

hygromycin-a

•

acids

•

methoxyhygromycin

•

aminocyclitols

•

valienamine

•

antibiotics

•

inhibitors

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LGSA  
Available on Infoscience
November 9, 2005
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/219649
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