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Highly efficient access to bi- and tricyclic ketals through gold-catalyzed tandem reactions of 4-acyl-1,6-diynes.

Authors :
Meng J
Zhao YL
Ren CQ
Li Y
Li Z
Liu Q
Source :
Chemistry (Weinheim an der Bergstrasse, Germany) [Chemistry] 2009; Vol. 15 (8), pp. 1830-4.
Publication Year :
2009

Abstract

Single step: Fused bicyclic and bridged tricyclic ketals were synthesized in a single step from the reactions of easily available 4-acyl-1,6-diynes with H(2)O and alkanols (see scheme). The highly efficient AuCl(3)-catalyzed multicomponent domino reactions, involving five C-O bond formations, can proceed in a highly regio- and diastereoselective manner at room temperature under air and lead to structures of high molecular complexity from simple starting materials in an atom economic way.

Details

Language :
English
ISSN :
1521-3765
Volume :
15
Issue :
8
Database :
MEDLINE
Journal :
Chemistry (Weinheim an der Bergstrasse, Germany)
Publication Type :
Academic Journal
Accession number :
19132708
Full Text :
https://doi.org/10.1002/chem.200802304