Application of a new nucleophilic addition/ring closure (NARC) sequence tothe synthesis of enantiomerically-pure 2,8-dioxabicyclo[3.2.1]octanes of relevance to the squalestatins and zaragozic acids

Authors
Fallon, GD Jones, ED Perlmutter, P Selajarern, W
Citation
Gd. Fallon et al., Application of a new nucleophilic addition/ring closure (NARC) sequence tothe synthesis of enantiomerically-pure 2,8-dioxabicyclo[3.2.1]octanes of relevance to the squalestatins and zaragozic acids, TETRAHEDR L, 40(41), 1999, pp. 7435-7438
Citations number
35
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
40
Issue
41
Year of publication
1999
Pages
7435 - 7438
Database
ISI
SICI code
0040-4039(19991008)40:41<7435:AOANNA>2.0.ZU;2-1
Abstract
PL rapid method for the enantioselective construction of 2,8-dioxabicyclo[3 .2.1]octanes of relevance to the zaragozic acids, employing a tandem NARC s equence of aldol and intramolecular Wacker reactions, is described. (C) 199 9 Published by Elsevier Science Ltd. All rights reserved.