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Synthesis 2014; 46(24): 3331-3340
DOI: 10.1055/s-0034-1379141
DOI: 10.1055/s-0034-1379141
paper
A New Route to Pyranocoumarins and Their Benzannulated Derivatives
Autor*innen
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Publikationsverlauf
Received: 29. Juni 2014
Accepted after revision: 20. August 2014
Publikationsdatum:
15. September 2014 (online)
Abstract
A new protocol based on sequential applications of three atom-economic processes viz. Claisen rearrangement, olefin isomerisation, and ring-closing diene metathesis has been developed to access a range of linear and angularly fused pyranocoumarin derivatives. Incorporation of enyne (in place of diene) metathesis and Diels–Alder reaction in the sequence has allowed the corresponding benzannulated derivatives to be prepared in good yields.
Supporting Information
- for this article is available online at http://www.thieme-connect.com/products/ejournals/journal/
10.1055/s-00000084.
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For some recent assorted reports, see:
For some recent reviews on isomerisation–RCM sequences, see:
For some recent reports, see:
For some reviews on RCEYM and related issues, see:
For some recent reports, see: