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Synthesis 2015; 47(09): 1317-1324
DOI: 10.1055/s-0034-1380130
DOI: 10.1055/s-0034-1380130
paper
On the Importance of the Relative Stereochemistry of Substituents in the Formation of Nine-Membered Lactones by Ring-Closing Metathesis
Further Information
Publication History
Received: 26 November 2014
Accepted after revision: 02 January 2015
Publication Date:
19 February 2015 (online)
Abstract
The effects of isopropyl substituents and molar concentration of diastereomeric esters toward the formation of nine-membered unsaturated lactones, in the context of the synthesis of the intermediates of the antihypertensive drug aliskiren, have been studied.
Supporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0034-1380130.
- Supporting Information
-
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See for example:
For selected reviews on using ring-closing metathesis in the synthesis of macrolactone natural products, see