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research article

Stereoselective synthesis of new conduramines and aminocyclitol derivatives

Jotterand, N.
•
Vogel, P.  
1998
Synlett

Triacetate of 7-oxabicyclo[2.2.1]hept-5-ene-1,2-exo,3-exo-trimethanol was converted selectively into (1RS,2SR,5RS,6RS)-4,5,6-tris(acetoxymethyl)-2-bromocyclohex-3-en-1-ol (4) or into (1RS,2SR,5RS,6RS)-5,6-bis(acetoxymethyl)-2-bromo-4-bromomethylcyclohex-3 -en-1-ol (12). These products were displaced with azide anion and transformed into (1RS,2RS,5RS,6RS)-2-amino-4,5,6-tris(hydroxymethyl)cyclohex-3-en-1-ol (7) and (1RS,2RS,5RS,6RS)-2-amino-4-aminomethyl-5,6-bis(hydroxymethyl)cyclohex-3 -en-1-ol (15), respectively. (1RS,2SR,3RS,4SR,5RS,6SR)-3-Amino-1,5,6-tris(hydroxymethyl)cyclohexa-1,2 ,4-triol (11) was also derived from 4.

  • Details
  • Metrics
Type
research article
DOI
10.1055/s-1998-1909
Author(s)
Jotterand, N.
Vogel, P.  
Date Issued

1998

Published in
Synlett
Issue

11

Start page

1237

End page

1239

Subjects

aminopolyols

•

diaminopolyols

•

glycosidase inhibitor

•

7-oxabicyclo[2.2.1]heptenes

•

S(N)2 ' ring opening

•

Site-directed inhibitors

•

pseudo-sugars

•

(phenylsulfonyl)-7-oxabicyclo<2.2.1>heptane derivatives

•

aminoglycoside

•

antibiotics

•

(+/-)-methyl shikimate

•

cis-dihydroxylation

•

rna

•

binding

•

ribozyme

•

analogs

Note

Univ Lausanne, Chim Sect, BCH, CH-1015 Lausanne, Switzerland.

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/20.500.14299/219734
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