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  4. An expeditious asymmetric synthesis of polyfunctional 1,7-dioxaspiro[5.5]undecanes
 
research article

An expeditious asymmetric synthesis of polyfunctional 1,7-dioxaspiro[5.5]undecanes

Gerber-Lemaire, S  
•
Vogel, P  
2004
European Journal of Organic Chemistry

Quick access to polyfunctional spiroketal (3R)-4-[(2S,6R,8R, 10S)-4,4-bis(ethylthio)-10-hydroxy-8-(2-hydroxyethyl)- 1,7-dioxaspiro[5.5]undec-2-yl]butane- 1,3-diol [(+)-19] is now available through the stereoselective functionalization of enantiomerically pure protected tetrol (4R,4'R,6R,6'R)- 1, l'-methylenebis[4-[(benzyloxy)methoxy]-6-[(triethylsilyl)-oxy]cyclohept- 1-ene [(-)-9], derived from 2,2'-methylenedifuran. (C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004).

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Type
research article
DOI
10.1002/ejoc.200400514
Web of Science ID

WOS:000225858100011

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

2004

Published in
European Journal of Organic Chemistry
Issue

24

Start page

5040

End page

5046

Subjects

spongistatin 1 altohyrtin

•

marine macrolide synthesis

•

formaltotal-synthesis

•

complex natural-products

•

sponge hyrtios-altum

•

enantioselective synthesis

•

stereocontrolled synthesis

•

spiroacetalportion

•

c spongistatin-2

•

2nd-generation construction

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/20.500.14299/219454
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