Literature DB >> 15957943

Alpha-hydroxy cyclopentenones from alpha-diketones.

William A Batson1, Divakaramenon Sethumadhavan, Marcus A Tius.   

Abstract

[reaction: see text] Metalloenolates derived from alpha,beta-unsaturated alpha-diketones undergo cyclization to alpha-hydroxy cyclopentenones. This is apparently the first reported Nazarov reaction that takes place in the presence of base.

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Year:  2005        PMID： 15957943     DOI： 10.1021/ol050970x

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


  4 in total

1.  An organocatalytic asymmetric Nazarov cyclization.

Authors:  Ashok K Basak; Naoyuki Shimada; William F Bow; David A Vicic; Marcus A Tius
Journal:  J Am Chem Soc       Date:  2010-06-23       Impact factor: 15.419

2.  Asymmetric Nazarov Cyclizations.

Authors:  Naoyuki Shimada; Craig Stewart; Marcus A Tius
Journal:  Tetrahedron       Date:  2011-08-19       Impact factor: 2.457

3.  Conjugate addition-initiated Nazarov cyclization.

Authors:  Joshua L Brooks; Patrick A Caruana; Alison J Frontier
Journal:  J Am Chem Soc       Date:  2011-07-22       Impact factor: 15.419

4.  Beyond the Divinyl Ketone: Innovations in the Generation and Nazarov Cyclization of Pentadienyl Cation Intermediates.

Authors:  William T Spencer; Tulaza Vaidya; Alison J Frontier
Journal:  European J Org Chem       Date:  2013-06-01
  4 in total

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