Literature DB >> 15547910

A highly stereoselective addition of the anion derived from alpha-diazoacetamide to aromatic N-tosylimines.

Yonghua Zhao1, Zhihua Ma, Xiaomei Zhang, Yaping Zou, Xianglin Jin, Jianbo Wang.   

Abstract

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Year:  2004        PMID： 15547910     DOI： 10.1002/anie.200460730

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN： 1433-7851            Impact factor:   15.336


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  3 in total

1.  A new reactivity mode for the diazo group: diastereoselective 1,3-aminoalkylation reaction of β-amino-α-diazoesters to give triazolines.

Authors:  Alexey Kuznetsov; Anton V Gulevich; Donald J Wink; Vladimir Gevorgyan
Journal:  Angew Chem Int Ed Engl       Date:  2014-07-01       Impact factor: 15.336

2.  Pyridine group assisted addition of diazo-compounds to imines in the 3-CC reaction of 2-aminopyridines, aldehydes, and diazo-compounds.

Authors:  Anton V Gulevich; Victoria Helan; Donald J Wink; Vladimir Gevorgyan
Journal:  Org Lett       Date:  2013-02-01       Impact factor: 6.005

3.  Asymmetric synthesis of diverse glycolic acid scaffolds via dynamic kinetic resolution of α-keto esters.

Authors:  Kimberly M Steward; Michael T Corbett; C Guy Goodman; Jeffrey S Johnson
Journal:  J Am Chem Soc       Date:  2012-11-27       Impact factor: 15.419
  3 in total

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