Literature DB >> 21919477

Marrying iterative synthesis to cascading radical cyclization: 6-endo/5-exo radical cascade across bis-vinyl ethers.

Katherine A Davies1, Jeremy E Wulff.   

Abstract

Application of iterative protocols to the synthesis of functionally and stereochemically complex small molecules is an emerging area of research with the potential to create new efficiencies in complex molecule synthesis. Similarly, the discovery of tandem or cascade reactions can aid in the rapid generation of new structures for biological screening programs. This report describes a cascading 6-endo-trig/5-exo-trig radical cyclization across bis-vinyl ether substrates, which are themselves iteratively synthesized from simple building blocks.
© 2011 American Chemical Society

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Year:  2011        PMID: 21919477     DOI: 10.1021/ol202286q

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Total synthesis of maoecrystal V: early-stage C-H functionalization and lactone assembly by radical cyclization.

Authors:  Ping Lu; Zhenhua Gu; Armen Zakarian
Journal:  J Am Chem Soc       Date:  2013-09-23       Impact factor: 15.419

2.  Enantioselective synthesis of (-)-maoecrystal V by enantiodetermining C-H functionalization.

Authors:  Ping Lu; Artur Mailyan; Zhenhua Gu; David M Guptill; Hengbin Wang; Huw M L Davies; Armen Zakarian
Journal:  J Am Chem Soc       Date:  2014-12-11       Impact factor: 15.419

  2 in total

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