Literature DB >> 22109267

Cross-coupling: The final frontier.

Ben W Glasspoole, Cathleen M Crudden.   

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Year:  2011        PMID： 22109267     DOI： 10.1038/nchem.1210

Source DB:  PubMed          Journal:  Nat Chem        ISSN： 1755-4330            Impact factor:   24.427


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  10 in total

1.  Suzuki cross-couplings of unactivated secondary alkyl bromides and iodides.

Authors:  Jianrong Zhou; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2004-02-11       Impact factor: 15.419

2.  Catalytic asymmetric γ-alkylation of carbonyl compounds via stereoconvergent Suzuki cross-couplings.

Authors:  Susan L Zultanski; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2011-09-13       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.  Asymmetric alkyl-alkyl cross-couplings of unactivated secondary alkyl electrophiles: stereoconvergent Suzuki reactions of racemic acylated halohydrins.

Authors:  Nathan A Owston; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2010-09-01       Impact factor: 15.419

5.  Enantioselective preparation and chemoselective cross-coupling of 1,1-diboron compounds.

Authors:  Jack Chang Hung Lee; Robert McDonald; Dennis G Hall
Journal:  Nat Chem       Date:  2011-09-25       Impact factor: 24.427

Review 6.  Catalytic, enantioselective, vinylogous aldol reactions.

Authors:  Scott E Denmark; John R Heemstra; Gregory L Beutner
Journal:  Angew Chem Int Ed Engl       Date:  2005-07-25       Impact factor: 15.336

7.  Stereospecific Suzuki-Miyaura coupling of chiral α-(acylamino)benzylboronic esters with inversion of configuration.

Authors:  Toshimichi Ohmura; Tomotsugu Awano; Michinori Suginome
Journal:  J Am Chem Soc       Date:  2010-09-29       Impact factor: 15.419

8.  Efficient cross-coupling of secondary alkyltrifluoroborates with aryl chlorides--reaction discovery using parallel microscale experimentation.

Authors:  Spencer D Dreher; Peter G Dormer; Deidre L Sandrock; Gary A Molander
Journal:  J Am Chem Soc       Date:  2008-06-27       Impact factor: 15.419

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 coupling reactions of chiral secondary organoboronic esters with retention of configuration.

Authors:  Daisuke Imao; Ben W Glasspoole; Véronique S Laberge; Cathleen M Crudden
Journal:  J Am Chem Soc       Date:  2009-04-15       Impact factor: 15.419
  10 in total
  12 in total

1.  Nickel-catalyzed coupling reactions of alkyl electrophiles, including unactivated tertiary halides, to generate carbon-boron bonds.

Authors:  Alexander S Dudnik; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2012-06-06       Impact factor: 15.419

Review 2.  Transition metal-catalyzed alkyl-alkyl bond formation: Another dimension in cross-coupling chemistry.

Authors:  Junwon Choi; Gregory C Fu
Journal:  Science       Date:  2017-04-14       Impact factor: 47.728

3.  Synthesis of [18F]-γ-fluoro-α,β,-unsaturated esters and ketones via vinylogous 18F-fluorination of α-diazoacetates with [18F]AgF.

Authors:  Stephen Thompson; So Jeong Lee; Isaac M Jackson; Naoko Ichiishi; Allen F Brooks; Melanie S Sanford; Peter J H Scott
Journal:  Synthesis (Stuttg)       Date:  2019-12       Impact factor: 3.157

4.  Catalytic enantioselective cross-couplings of secondary alkyl electrophiles with secondary alkylmetal nucleophiles: Negishi reactions of racemic benzylic bromides with achiral alkylzinc reagents.

Authors:  Jörg T Binder; Christopher J Cordier; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2012-10-05       Impact factor: 15.419

5.  A mild, palladium-catalyzed method for the dehydrohalogenation of alkyl bromides: synthetic and mechanistic studies.

Authors:  Alex C Bissember; Anna Levina; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2012-08-20       Impact factor: 15.419

6.  Nickel-catalyzed carbon-carbon bond-forming reactions of unactivated tertiary alkyl halides: Suzuki arylations.

Authors:  Susan L Zultanski; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2013-01-02       Impact factor: 15.419

7.  Enantioconvergent cross-couplings of racemic alkylmetal reagents with unactivated secondary alkyl electrophiles: catalytic asymmetric Negishi α-alkylations of N-Boc-pyrrolidine.

Authors:  Christopher J Cordier; Rylan J Lundgren; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2013-07-19       Impact factor: 15.419

8.  Copper(I)-Catalyzed Asymmetric Conjugate 1,6-, 1,8-, and 1,10-Borylation.

Authors:  Chang-Yun Shi; Jungmin Eun; Timothy R Newhouse; Liang Yin
Journal:  Angew Chem Int Ed Engl       Date:  2021-03-18       Impact factor: 15.336

9.  Nickel-catalyzed Negishi arylations of propargylic bromides: a mechanistic investigation.

Authors:  Nathan D Schley; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2014-11-17       Impact factor: 15.419

10.  Catalytic enantioselective cyclization/cross-coupling with alkyl electrophiles.

Authors:  Huan Cong; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2014-02-27       Impact factor: 15.419
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