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  4. An expeditious, non-iterative, and asymmetric synthesis of 3,5,7,9,11,13,15-heptahydroxypentadecanals
 
research article

An expeditious, non-iterative, and asymmetric synthesis of 3,5,7,9,11,13,15-heptahydroxypentadecanals

Gerber-Lemaire, S  
•
Vogel, P  
2003
European Journal of Organic Chemistry

Ozonolysis of (1R,1'R,6R,6'R)-3,3'-methylenebis{6-[(benzyloxy)methoxy]cyclohept-3-en-1 -ol} followed by the diastereo-selective reduction of the resulting beta-hydroxy ketone intermediates gives a rapid route to long-chain polyketides bearing unsymmetrical functions at their terminal positions. These can easily be converted into enantiomerically pure long-chain 1,3-polyol fragments. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003).

  • Details
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Type
research article
DOI
10.1002/ejoc.200300224
Web of Science ID

WOS:000184500800026

Author(s)
Gerber-Lemaire, S  
Vogel, P  
Date Issued

2003

Published in
European Journal of Organic Chemistry
Issue

15

Start page

2959

End page

2963

Subjects

polyene macrolide antibiotics

•

delta-valerolactones

•

enantioselectivesynthesis

•

stereoselective-synthesis

•

building-blocks

•

lactone moiety

•

amphotericin-b

•

mevinic acid

•

chain

•

8-oxabicyclo<3.2.1>oct-6-en-3-one

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/20.500.14299/219452
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