Literature DB >> 21533010

NICKEL-CATALYZED ENANTIOSELECTIVE NEGISHI CROSS-COUPLINGS OF RACEMIC SECONDARY α-BROMO AMIDES WITH ALKYLZINC REAGENTS: (S)-N-BENZYL-7-CYANO-2-ETHYL-N-PHENYLHEPTANAMIDE.

Sha Lou1, Gregory C Fu.   

Abstract

Entities:  

Year:  2010        PMID： 21533010      PMCID： PMC3083032     

Source DB:  PubMed          Journal:  Organic Synth        ISSN： 0078-6209


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  15 in total

1.  Enantioselective suzuki reactions: catalytic asymmetric synthesis of compounds containing quaternary carbon centers.

Authors:  Michael C Willis; Luke H W Powell; Christelle K Claverie; Simon J Watson
Journal:  Angew Chem Int Ed Engl       Date:  2004-02-27       Impact factor: 15.336

2.  Catalysts for cross-coupling reactions with non-activated alkyl halides.

Authors:  Anja C Frisch; Matthias Beller
Journal:  Angew Chem Int Ed Engl       Date:  2005-01-21       Impact factor: 15.336

3.  Catalytic enantioselective Negishi reactions of racemic secondary benzylic halides.

Authors:  Forrest O Arp; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2005-08-03       Impact factor: 15.419

4.  Asymmetric nickel-catalyzed Negishi cross-couplings of secondary alpha-bromo amides with organozinc reagents.

Authors:  Christian Fischer; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2005-04-06       Impact factor: 15.419

5.  Catalytic asymmetric Hiyama cross-couplings of racemic alpha-bromo esters.

Authors:  Xing Dai; Neil A Strotman; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2008-02-27       Impact factor: 15.419

Review 6.  Secondary alkyl halides in transition-metal-catalyzed cross-coupling reactions.

Authors:  Alena Rudolph; Mark Lautens
Journal:  Angew Chem Int Ed Engl       Date:  2009       Impact factor: 15.336

7.  An improved catalyst for the asymmetric arylation of ketone enolates.

Authors:  Takayuki Hamada; André Chieffi; Jens Ahman; Stephen L Buchwald
Journal:  J Am Chem Soc       Date:  2002-02-20       Impact factor: 15.419

8.  Catalytic asymmetric cross-couplings of racemic alpha-bromoketones with arylzinc reagents.

Authors:  Pamela M Lundin; Jorge Esquivias; Gregory C Fu
Journal:  Angew Chem Int Ed Engl       Date:  2009       Impact factor: 15.336

9.  Enantioselective alkyl-alkyl Suzuki cross-couplings of unactivated homobenzylic halides.

Authors:  Bunnai Saito; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2008-05-01       Impact factor: 15.419

10.  Cross-couplings of unactivated secondary alkyl halides: room-temperature nickel-catalyzed Negishi reactions of alkyl bromides and iodides.

Authors:  Jianrong Steve Zhou; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2003-12-03       Impact factor: 15.419
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  4 in total

Review 1.  The Fascinating Chemistry of α-Haloamides.

Authors:  Anna Fantinati; Vinicio Zanirato; Paolo Marchetti; Claudio Trapella
Journal:  ChemistryOpen       Date:  2020-01-13       Impact factor: 2.911

2.  Nickel-catalyzed enantioselective cross-couplings of racemic secondary electrophiles that bear an oxygen leaving group.

Authors:  Alexander J Oelke; Jianwei Sun; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2012-02-01       Impact factor: 15.419

3.  Stereoconvergent amine-directed alkyl-alkyl Suzuki reactions of unactivated secondary alkyl chlorides.

Authors:  Zhe Lu; Ashraf Wilsily; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2011-05-10       Impact factor: 15.419

4.  A general, modular method for the catalytic asymmetric synthesis of alkylboronate esters.

Authors:  Jens Schmidt; Junwon Choi; Albert Tianxiang Liu; Martin Slusarczyk; Gregory C Fu
Journal:  Science       Date:  2016-12-08       Impact factor: 47.728
  4 in total

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