Literature DB >> 12790620

Highly regioselective ring opening of oxiranes with phenoxides in the presence of beta-cyclodextrin in water.

K Surendra1, N Srilakshmi Krishnaveni, Y V D Nageswar, K Rama Rao.   

Abstract

Highly regioselective ring opening of oxiranes to beta-hydroxy ethers with phenoxides has been achieved in impressive yields in the presence of beta-cyclodextrin as catalyst and water as solvent.

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Year:  2003        PMID： 12790620     DOI： 10.1021/jo034194n

Source DB:  PubMed          Journal:  J Org Chem        ISSN： 0022-3263            Impact factor:   4.354


  2 in total

1.  Chiral epoxides via borane reduction of 2-haloketones catalyzed by spiroborate ester: application to the synthesis of optically pure 1,2-hydroxy ethers and 1,2-azido alcohols.

Authors:  Kun Huang; Haiyang Wang; Viatcheslav Stepanenko; Melvin De Jesús; Carilyn Torruellas; Wildeliz Correa; Margarita Ortiz-Marciales
Journal:  J Org Chem       Date:  2011-02-04       Impact factor: 4.354

2.  Discovery, synthesis, and biological evaluation of piperidinol analogs with anti-tuberculosis activity.

Authors:  Dianqing Sun; Michael S Scherman; Victoria Jones; Julian G Hurdle; Lisa K Woolhiser; Susan E Knudson; Anne J Lenaerts; Richard A Slayden; Michael R McNeil; Richard E Lee
Journal:  Bioorg Med Chem       Date:  2009-04-09       Impact factor: 3.641
  2 in total

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