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Recent applications in natural product synthesis of dihydrofuran and -pyran formation by ring-closing alkene metathesis.

Authors :
Jacques R
Pal R
Parker NA
Sear CE
Smith PW
Ribaucourt A
Hodgson DM
Source :
Organic & biomolecular chemistry [Org Biomol Chem] 2016 Jul 07; Vol. 14 (25), pp. 5875-93. Date of Electronic Publication: 2016 Apr 25.
Publication Year :
2016

Abstract

In the past two decades, alkene metathesis has risen in prominence to become a significant synthetic strategy for alkene formation. Many total syntheses of natural products have used this transformation. We review the use, from 2003 to 2015, of ring-closing alkene metathesis (RCM) for the generation of dihydrofurans or -pyrans in natural product synthesis. The strategies used to assemble the RCM precursors and the subsequent use of the newly formed unsaturation will also be highlighted and placed in context.

Details

Language :
English
ISSN :
1477-0539
Volume :
14
Issue :
25
Database :
MEDLINE
Journal :
Organic & biomolecular chemistry
Publication Type :
Academic Journal
Accession number :
27108941
Full Text :
https://doi.org/10.1039/c6ob00593d