Literature DB >> 11456846

Stereoselective generation of E- and Z-disubstituted amide enolates. Reductive enolate formation from bicyclic thioglycolate lactams.

J M Manthorpe, J L Gleason.   

Abstract

Entities:  

Year:  2001        PMID： 11456846     DOI： 10.1021/ja0058280

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN： 0002-7863            Impact factor:   15.419


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  10 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.  A unique approach to aldol products for the creation of all-carbon quaternary stereocentres.

Authors:  Jaya Prakash Das; Helena Chechik; Ilan Marek
Journal:  Nat Chem       Date:  2009-03-29       Impact factor: 24.427

3.  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

4.  Total synthesis of pinnatoxins A and G and revision of the mode of action of pinnatoxin A.

Authors:  Romulo Araoz; Denis Servent; Jordi Molgó; Bogdan I Iorga; Carole Fruchart-Gaillard; Evelyne Benoit; Zhenhua Gu; Craig Stivala; Armen Zakarian
Journal:  J Am Chem Soc       Date:  2011-06-17       Impact factor: 15.419

5.  Forming all-carbon quaternary stereogenic centres in acyclic systems from alkynes.

Authors:  Yury Minko; Morgane Pasco; Lukas Lercher; Mark Botoshansky; Ilan Marek
Journal:  Nature       Date:  2012-10-25       Impact factor: 49.962

6.  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

7.  Silyl ketene imines: highly versatile nucleophiles for catalytic, asymmetric synthesis.

Authors:  Scott E Denmark; Tyler W Wilson
Journal:  Angew Chem Int Ed Engl       Date:  2012-09-11       Impact factor: 15.336

8.  Catalytic Enantioselective Synthesis of Acyclic Quaternary Centers: Palladium-Catalyzed Decarboxylative Allylic Alkylation of Fully Substituted Acyclic Enol Carbonates.

Authors:  Eric J Alexy; Haiming Zhang; Brian M Stoltz
Journal:  J Am Chem Soc       Date:  2018-08-02       Impact factor: 15.419

9.  Stereodefined trisubstituted enolates as a unique entry to all-carbon quaternary stereogenic centers in acyclic systems.

Authors:  Yury Minko; Morgane Pasco; Lukas Lercher; Ilan Marek
Journal:  Nat Protoc       Date:  2013-03-21       Impact factor: 13.491

10.  Asymmetric synthesis of γ-chloro-α,β-diamino- and β,γ-aziridino-α-aminoacylpyrrolidines and -piperidines via stereoselective Mannich-type additions of N-(diphenylmethylene)glycinamides across α-chloro-N-sulfinylimines.

Authors:  Gert Callebaut; Sven Mangelinckx; Pieter Van der Veken; Karl W Törnroos; Koen Augustyns; Norbert De Kimpe
Journal:  Beilstein J Org Chem       Date:  2012-12-05       Impact factor: 2.883
  10 in total

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