Literature DB >> 20715038

Alkyl-alkyl Suzuki cross-coupling of unactivated secondary alkyl chlorides.

Zhe Lu1, Gregory C Fu.   

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Year:  2010        PMID: 20715038      PMCID: PMC3073318          DOI: 10.1002/anie.201003272

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


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  9 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.  Amino alcohols as ligands for nickel-catalyzed suzuki reactions of unactivated alkyl halides, including secondary alkyl chlorides, with arylboronic acids.

Authors:  Francisco González-Bobes; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2006-04-26       Impact factor: 15.419

Review 3.  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

4.  Ligand redox effects in the synthesis, electronic structure, and reactivity of an alkyl-alkyl cross-coupling catalyst.

Authors:  Gavin D Jones; Jason L Martin; Chris McFarland; Olivia R Allen; Ryan E Hall; Aireal D Haley; R Jacob Brandon; Tatyana Konovalova; Patrick J Desrochers; Peter Pulay; David A Vicic
Journal:  J Am Chem Soc       Date:  2006-10-11       Impact factor: 15.419

5.  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

6.  Density functional theory studies of negishi alkyl-alkyl cross-coupling reactions catalyzed by a methylterpyridyl-Ni(I) complex.

Authors:  Xufeng Lin; David Lee Phillips
Journal:  J Org Chem       Date:  2008-04-15       Impact factor: 4.354

7.  A concise and modular synthesis of pyranicin.

Authors:  Nolan D Griggs; Andrew J Phillips
Journal:  Org Lett       Date:  2008-10-10       Impact factor: 6.005

8.  A cyclopropanol-based strategy for subunit coupling: total synthesis of (+)-spirolaxine methyl ether.

Authors:  Katie A Keaton; Andrew J Phillips
Journal:  Org Lett       Date:  2007-06-09       Impact factor: 6.005

9.  Alkyl-alkyl suzuki cross-couplings of unactivated secondary alkyl halides at room temperature.

Authors:  Bunnai Saito; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2007-07-12       Impact factor: 15.419

  9 in total
  14 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

2.  Distinguishing between pathways for transmetalation in Suzuki-Miyaura reactions.

Authors:  Brad P Carrow; John F Hartwig
Journal:  J Am Chem Soc       Date:  2011-01-31       Impact factor: 15.419

Review 3.  Advances in transition metal (Pd, Ni, Fe)-catalyzed cross-coupling reactions using alkyl-organometallics as reaction partners.

Authors:  Ranjan Jana; Tejas P Pathak; Matthew S Sigman
Journal:  Chem Rev       Date:  2011-02-14       Impact factor: 60.622

4.  Cross-Electrophile Coupling of Unactivated Alkyl Chlorides.

Authors:  Holt A Sakai; Wei Liu; Chi Chip Le; David W C MacMillan
Journal:  J Am Chem Soc       Date:  2020-06-26       Impact factor: 15.419

5.  Asymmetric transition metal-catalyzed cross-coupling reactions for the construction of tertiary stereocenters.

Authors:  Elizabeth C Swift; Elizabeth R Jarvo
Journal:  Tetrahedron       Date:  2013-07-22       Impact factor: 2.457

6.  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

7.  Synthesis of Secondary and Tertiary Alkylboranes via Formal Hydroboration of Terminal and 1,1-Disubstituted Alkenes.

Authors:  Hilary A Kerchner; John Montgomery
Journal:  Org Lett       Date:  2016-10-27       Impact factor: 6.005

8.  Expanded substrate scope and improved reactivity of ether-forming cross-coupling reactions of organotrifluoroborates and acetals.

Authors:  Cam-Van T Vo; T Andrew Mitchell; Jeffrey W Bode
Journal:  J Am Chem Soc       Date:  2011-08-17       Impact factor: 15.419

9.  Monovalent Nickel-Mediated Radical Formation: A Concerted Halogen-Atom Dissociation Pathway Determined by Electroanalytical Studies.

Authors:  Qiao Lin; Yue Fu; Peng Liu; Tianning Diao
Journal:  J Am Chem Soc       Date:  2021-08-25       Impact factor: 15.419

10.  Ti-Catalyzed Radical Alkylation of Secondary and Tertiary Alkyl Chlorides Using Michael Acceptors.

Authors:  Xiangyu Wu; Wei Hao; Ke-Yin Ye; Binyang Jiang; Gisselle Pombar; Zhidong Song; Song Lin
Journal:  J Am Chem Soc       Date:  2018-10-26       Impact factor: 15.419

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