Literature DB >> 21858348

Practical and stereoselective synthesis of β-amino sulfones from alkyl phenyl sulfones and N-(tert-butylsulfinyl) aldimines.

Hua Zhang1, Ya Li, Wei Xu, Wenrui Zheng, Pei Zhou, Zhihua Sun.   

Abstract

A practical and straightforward approach for the highly stereoselective synthesis of β-amino sulfones was developed. With lithium bis(trimethylsilyl)amide as the base, the corresponding sulfone-stabilized carbanion derived from alkylphenyl sulfone can be transferred to N-(tert-butylsulfinyl) aldimines in excellent yields and with high diastereoselectivity.

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Year:  2011        PMID: 21858348     DOI: 10.1039/c1ob05992k

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

1.  (R)-N-[(R)-2,2-Di-chloro-1-phenyl-2-(phenyl-sulfon-yl)eth-yl]-2-methyl-propane-2-sulfinamide.

Authors:  Haiji Huang; Ya Li; Jingming Chu
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2014-01-08
  1 in total

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