Literature DB >> 10823209

Simple and practical routes to enantiomerically pure 5-(trialkylsilyl)-2-cyclohexenones.

G Sarakinos1, E J Corey.   

Abstract

[reaction: see text] Enantiomerically pure chiral 5-silylated 2-cyclohexenones are easily prepared in high yield using as a key step kinetic resolution with a commercially available lipase. Fully active enzyme can be recovered very efficiently for reuse. The synthetic steps are outlined in Schemes 1 and 3. Enantiomerically pure 2-cyclohexenones such as 1 and 2 are versatile intermediates for the synthesis of a multitude of chiral targets by means of a variety of diastereoselective reactions such as those illustrated in Scheme 2.

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Year:  1999        PMID: 10823209     DOI: 10.1021/ol990805f

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


  2 in total

Review 1.  Polycyclic Furanobutenolide-Derived Cembranoid and Norcembranoid Natural Products: Biosynthetic Connections and Synthetic Efforts.

Authors:  Robert A Craig; Brian M Stoltz
Journal:  Chem Rev       Date:  2017-05-18       Impact factor: 60.622

2.  A short and efficient synthesis of (-)-7-methylomuralide, a potent proteasome inhibitor.

Authors:  Ryan A Shenvi; E J Corey
Journal:  J Am Chem Soc       Date:  2009-04-29       Impact factor: 15.419

  2 in total

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