Literature DB >> 21417438

Asymmetric synthesis of anti-α-substituted β-amino ketones from sulfinimines.

Franklin A Davis1, Peng Xu.   

Abstract

Previously unknown, enantiopure, β-amino ketones were prepared in modest yield by addition of lithium reagents to N-sulfinyl anti-α-substituted β-amino Weinreb amides. Grignard reagents failed to add to these Weinreb amides in contrast to the syn-α-substituted isomers which did. The anti-α-substituted β-amino Weinreb amides were prepared by addition of LiN(OMe)Me to the corresponding N-sulfinyl anti-α-substituted β-amino esters because α-alkylation of N-sulfinyl β-amino Weinreb amide enolates resulted in poor diastereoselectivities.
© 2011 American Chemical Society

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Year:  2011        PMID: 21417438     DOI: 10.1021/jo2002352

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


  3 in total

1.  Lithium Enolates Derived from Weinreb Amides: Insights into Five-Membered Chelate Rings.

Authors:  Michael J Houghton; David B Collum
Journal:  J Org Chem       Date:  2016-10-17       Impact factor: 4.354

2.  β-Amino functionalization of cinnamic Weinreb amides in ionic liquid.

Authors:  Yi-Ning Wang; Guo-Xiang Sun; Gang Qi
Journal:  Beilstein J Org Chem       Date:  2016-11-11       Impact factor: 2.883

3.  Efficient synthesis of β'-amino-α,β-unsaturated ketones.

Authors:  Isabelle Abrunhosa-Thomas; Aurélie Plas; Nishanth Kandepedu; Pierre Chalard; Yves Troin
Journal:  Beilstein J Org Chem       Date:  2013-03-06       Impact factor: 2.883

  3 in total

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