Literature DB >> 34463502

Stereospecific Nickel-Catalyzed Reductive Cross-Coupling of Alkyl Tosylate and Allyl Alcohol Electrophiles.

Quentin D Tercenio1, Erik J Alexanian1.   

Abstract

The stereospecific cross-coupling of easily accessed electrophiles holds significant promise in the construction of C-C bonds. Herein, we report a nickel-catalyzed reductive coupling of allyl alcohols with chiral, nonracemic alkyl tosylates. This cross-coupling delivers valuable allylation products with high levels of stereospecificity across a range of substrates. The catalytic system consists of a simple nickel salt in conjunction with a commercially available reductant and importantly represents a rare example of a cross-coupling involving the C-O bonds of two electrophiles.

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Year:  2021        PMID: 34463502      PMCID: PMC8734645          DOI: 10.1021/acs.orglett.1c02616

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.072


  32 in total

1.  Copper-Catalyzed Cross-Coupling Reaction of Allyl Boron Ester with 1°/2°/3°-Halogenated Alkanes.

Authors:  Guang-Zu Wang; Jian Jiang; Xiao-Song Bu; Jian-Jun Dai; Jun Xu; Yao Fu; Hua-Jian Xu
Journal:  Org Lett       Date:  2015-07-16       Impact factor: 6.005

2.  Reductive cross-coupling reactions between two electrophiles.

Authors:  Christiane E I Knappke; Sabine Grupe; Dominik Gärtner; Martin Corpet; Corinne Gosmini; Axel Jacobi von Wangelin
Journal:  Chemistry       Date:  2014-05-13       Impact factor: 5.236

3.  Cobalt-Catalyzed Carbonylative Cross-Coupling of Alkyl Tosylates and Dienes: Stereospecific Synthesis of Dienones at Low Pressure.

Authors:  Brendon T Sargent; Erik J Alexanian
Journal:  J Am Chem Soc       Date:  2017-08-29       Impact factor: 15.419

4.  Cobalt-catalyzed reductive allylation of alkyl halides with allylic acetates or carbonates.

Authors:  Xin Qian; Audrey Auffrant; Abdellah Felouat; Corinne Gosmini
Journal:  Angew Chem Int Ed Engl       Date:  2011-09-14       Impact factor: 15.336

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.  Nickel-catalyzed cross-coupling reaction of grignard reagents with alkyl halides and tosylates: remarkable effect of 1,3-butadienes.

Authors:  Jun Terao; Hideyuki Watanabe; Aki Ikumi; Hitoshi Kuniyasu; Nobuaki Kambe
Journal:  J Am Chem Soc       Date:  2002-04-24       Impact factor: 15.419

7.  Selective cross-coupling of organic halides with allylic acetates.

Authors:  Lukiana L Anka-Lufford; Michael R Prinsell; Daniel J Weix
Journal:  J Org Chem       Date:  2012-11-06       Impact factor: 4.354

8.  Ni- or Cu-catalyzed cross-coupling reaction of alkyl fluorides with Grignard reagents.

Authors:  Jun Terao; Aki Ikumi; Hitoshi Kuniyasu; Nobuaki Kambe
Journal:  J Am Chem Soc       Date:  2003-05-14       Impact factor: 15.419

9.  Stereospecific Intramolecular Reductive Cross-Electrophile Coupling Reactions for Cyclopropane Synthesis.

Authors:  Emily J Tollefson; Lucas W Erickson; Elizabeth R Jarvo
Journal:  J Am Chem Soc       Date:  2015-07-31       Impact factor: 15.419

10.  Cross-coupling reaction of alkyl halides with grignard reagents catalyzed by Ni, Pd, or Cu complexes with pi-carbon ligand(s).

Authors:  Jun Terao; Nobuaki Kambe
Journal:  Acc Chem Res       Date:  2008-11-18       Impact factor: 22.384

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  1 in total

1.  Organocatalytic Enantioselective α-Bromination of Aldehydes with N-Bromosuccinimide.

Authors:  George Hutchinson; Carla Alamillo-Ferrer; Martín Fernández-Pascual; Jordi Burés
Journal:  J Org Chem       Date:  2022-05-26       Impact factor: 4.198

  1 in total

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