Literature DB >> 21854012

Intramolecular aryne-ene reaction: synthetic and mechanistic studies.

David A Candito1, Jane Panteleev, Mark Lautens.   

Abstract

Although the chemistry of arynes is well developed, some challenges still remain. The ene reaction of arynes has not gained widespread use in synthesis as a result of poor yields and selectivity. A general, high yielding and selective intramolecular aryne-ene reaction is described providing various benzofused carbo- and heterocycles. Mechanistic data is presented, and a rationale for the resulting stereochemistry is discussed.

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Year:  2011        PMID: 21854012     DOI: 10.1021/ja205405n

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  4 in total

1.  Total syntheses of indolactam alkaloids (-)-indolactam V, (-)-pendolmycin, (-)-lyngbyatoxin A, and (-)-teleocidin A-2.

Authors:  Noah F Fine Nathel; Tejas K Shah; Sarah M Bronner; Neil K Garg
Journal:  Chem Sci       Date:  2014-06-01       Impact factor: 9.825

2.  Mechanism of the reactions of alcohols with o-benzynes.

Authors:  Patrick H Willoughby; Dawen Niu; Tao Wang; Moriana K Haj; Christopher J Cramer; Thomas R Hoye
Journal:  J Am Chem Soc       Date:  2014-09-17       Impact factor: 15.419

3.  The aromatic ene reaction.

Authors:  Dawen Niu; Thomas R Hoye
Journal:  Nat Chem       Date:  2013-11-17       Impact factor: 24.427

4.  δ-Deuterium isotope effects as probes for transition-state structures of isoprenoid substrates.

Authors:  Seoung-ryoung Choi; Martin Breugst; Kendall N Houk; C Dale Poulter
Journal:  J Org Chem       Date:  2014-04-01       Impact factor: 4.354

  4 in total

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