Literature DB >> 12203585

Stereoselective formation of quaternary carbon centers: alkylation of alpha,alpha-disubstituted amide enolates.

Jeffrey M Manthorpe1, James L Gleason.   

Abstract

Entities:  

Year:  2002        PMID： 12203585     DOI： 10.1002/1521-3773(20020703)41:13<2338::AID-ANIE2338>3.0.CO;2-M

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


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  3 in total

1.  Generation of stereochemically defined tetrasubstituted enolborinates by 1,4-hydroboration of α,β-unsaturated morpholine carboxamides with (diisopinocampheyl)borane.

Authors:  Christophe Allais; Andy S Tsai; Philippe Nuhant; William R Roush
Journal:  Angew Chem Int Ed Engl       Date:  2013-10-15       Impact factor: 15.336

2.  Enantioselective Construction of Acyclic Quaternary Carbon Stereocenters: Palladium-Catalyzed Decarboxylative Allylic Alkylation of Fully Substituted Amide Enolates.

Authors:  Pavel Starkov; Jared T Moore; Douglas C Duquette; Brian M Stoltz; Ilan Marek
Journal:  J Am Chem Soc       Date:  2017-07-07       Impact factor: 15.419

3.  Stereocontrolled alkylative construction of quaternary carbon centers.

Authors:  David A Kummer; William J Chain; Marvin R Morales; Olga Quiroga; Andrew G Myers
Journal:  J Am Chem Soc       Date:  2008-09-13       Impact factor: 15.419
  3 in total

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