Back to Search Start Over

Evolution of Total Syntheses of β‐Hydroxy‐γ‐Lactones: Cardiobutanolide and Hagen's Gland Lactones.

Authors :
Fernandes, Rodney A.
Kattanguru, Pullaiah
Halle, Mahesh B.
Kunkalkar, Rupesh A.
Source :
ChemistrySelect. 7/31/2017, Vol. 2 Issue 22, p6503-6518. 16p.
Publication Year :
2017

Abstract

Abstract: The β‐hydroxy‐γ‐lactones, cardiobutanolide and Hagen's gland lactones have been interesting targets for total synthesis in many laboratories. There are 10 syntheses reported for cardiobutanolide and 19 syntheses for Hagen's gland lactones. These natural products have the β‐hydroxy‐γ‐lactone moiety in common. The evolution of various synthetic strategies to these natural products from chiral pool materials and/or asymmetric catalysis and involving linear sequences, convergent approaches to the de‐novo protecting group free syntheses have been abstracted in this review. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
23656549
Volume :
2
Issue :
22
Database :
Academic Search Index
Journal :
ChemistrySelect
Publication Type :
Academic Journal
Accession number :
130770474
Full Text :
https://doi.org/10.1002/slct.201700862