Literature DB >> 11039527

Highly enantiomerically enriched alpha-haloalkyl Grignard reagents

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Abstract

alpha-Chloro- and alpha-bromoalkyl Grignard reagents 11 and 30 with > 97% ee (enantiomeric excess) were generated by a sulfoxide/magnesium exchange reaction from the enantiomerically and diastereomerically pure sulfoxides 25 and 27. The resulting alpha-haloalkyl Grignard reagents are configurationally stable at -78 degrees C. Racemization sets in at or above -60 degrees C, especially when the solution contains bromide ions. In the absence of halide ions, the configurational stability extends up to -20 degrees C, when chemical decomposition commences.

Entities:  

Year:  2000        PMID: 11039527     DOI: 10.1002/1521-3765(20000915)6:18<3359::aid-chem3359>3.0.co;2-u

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  1 in total

1.  Enantioselective assembly of tertiary stereocenters via multicomponent chemoselective cross-coupling of geminal chloro(iodo)alkanes.

Authors:  X Jiang; K Kulbitski; G Nisnevich; M Gandelman
Journal:  Chem Sci       Date:  2016-01-06       Impact factor: 9.825

  1 in total

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