Literature DB >> 33986970

Nickel-Catalyzed, Stereospecific C-C and C-B Cross-Couplings via C-N and C-O Bond Activation.

Jianyu Xu1, Olivia P Bercher1, Michael R Talley1, Mary P Watson1.   

Abstract

Highly enantioenriched benzylic and allylic amines and alcohols are readily available via asymmetric synthesis and in complex natural products. The development of mild, nickel-catalyzed cross-couplings of their derivatives has advanced the tools available for the preparation of a range of highly enantioenriched products, including those with quaternary stereocenters. This perspective focuses on cross-couplings with convenient and functional group-tolerant organoboron reagents and highlights the discoveries of activating groups and conditions that have led to high-yielding and highly stereospecific reactions. Emphasis is placed on mechanistic understanding, particularly with regards to controlling inversion vs. retention pathways. Limitations and opportunities for future developments are also highlighted.

Entities:  

Keywords:  Alcohols; Amines; Cross-couplings; Nickel Catalysis; Organoboron; Stereospecific

Year:  2021        PMID: 33986970      PMCID: PMC8112725          DOI: 10.1021/acscatal.0c05484

Source DB:  PubMed          Journal:  ACS Catal            Impact factor:   13.084


  43 in total

1.  Visible-Light-Driven External-Reductant-Free Cross-Electrophile Couplings of Tetraalkyl Ammonium Salts.

Authors:  Li-Li Liao; Guang-Mei Cao; Jian-Heng Ye; Guo-Quan Sun; Wen-Jun Zhou; Yong-Yuan Gui; Si-Shun Yan; Guo Shen; Da-Gang Yu
Journal:  J Am Chem Soc       Date:  2018-12-07       Impact factor: 15.419

2.  A General, Simple Catalyst for Enantiospecific Cross Couplings of Benzylic Ammonium Triflates and Boronic Acids: No Phosphine Ligand Required.

Authors:  Danielle M Shacklady-McAtee; Kelsey M Roberts; Corey H Basch; Ye-Geun Song; Mary P Watson
Journal:  Tetrahedron       Date:  2014-07-08       Impact factor: 2.457

3.  Stereospecific, Nickel-Catalyzed Suzuki-Miyaura Cross-Coupling of Allylic Pivalates To Deliver Quaternary Stereocenters.

Authors:  Kelsey M Cobb; Javon M Rabb-Lynch; Megan E Hoerrner; Alex Manders; Qi Zhou; Mary P Watson
Journal:  Org Lett       Date:  2017-08-07       Impact factor: 6.005

4.  Pd-catalyzed regioselective and stereospecific Suzuki-Miyaura coupling of allylic carbonates with arylboronic acids.

Authors:  Chenguang Li; Juxiang Xing; Jingming Zhao; Patrick Huynh; Wanbin Zhang; Pingkai Jiang; Yong Jian Zhang
Journal:  Org Lett       Date:  2011-12-20       Impact factor: 6.005

5.  Nickel-Catalyzed Borylation of Aryl- and Benzyltrimethylammonium Salts via C-N Bond Cleavage.

Authors:  Jiefeng Hu; Heqing Sun; Wangshui Cai; Xinghui Pu; Yemin Zhang; Zhuangzhi Shi
Journal:  J Org Chem       Date:  2015-12-15       Impact factor: 4.354

6.  Stereospecific nickel-catalyzed cross-coupling reactions of alkyl ethers: enantioselective synthesis of diarylethanes.

Authors:  Buck L H Taylor; Elizabeth C Swift; Joshua D Waetzig; Elizabeth R Jarvo
Journal:  J Am Chem Soc       Date:  2010-12-14       Impact factor: 15.419

7.  Nickel-catalyzed cross-couplings of benzylic pivalates with arylboroxines: stereospecific formation of diarylalkanes and triarylmethanes.

Authors:  Qi Zhou; Harathi D Srinivas; Srimoyee Dasgupta; Mary P Watson
Journal:  J Am Chem Soc       Date:  2013-02-20       Impact factor: 15.419

8.  A practical catalytic asymmetric addition of alkyl groups to ketones.

Authors:  Celina García; Lynne K LaRochelle; Patrick J Walsh
Journal:  J Am Chem Soc       Date:  2002-09-18       Impact factor: 15.419

Review 9.  Transition-Metal Catalysis of Nucleophilic Substitution Reactions: A Radical Alternative to SN1 and SN2 Processes.

Authors:  Gregory C Fu
Journal:  ACS Cent Sci       Date:  2017-06-12       Impact factor: 14.553

10.  Quaternary stereocentres via an enantioconvergent catalytic SN1 reaction.

Authors:  Alison E Wendlandt; Prithvi Vangal; Eric N Jacobsen
Journal:  Nature       Date:  2018-04-25       Impact factor: 49.962

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  6 in total

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

Authors:  Quentin D Tercenio; Erik J Alexanian
Journal:  Org Lett       Date:  2021-08-31       Impact factor: 6.072

2.  Visible-light-induced cross-coupling of aryl iodides with hydrazones via an EDA-complex.

Authors:  Pan Pan; Shihan Liu; Yu Lan; Huiying Zeng; Chao-Jun Li
Journal:  Chem Sci       Date:  2022-05-23       Impact factor: 9.969

3.  Dissection of Alkylpyridinium Structures to Understand Deamination Reactions.

Authors:  Sergei Tcyrulnikov; Qiuqi Cai; J Cameron Twitty; Jianyu Xu; Abderrahman Atifi; Olivia P Bercher; Glenn P A Yap; Joel Rosenthal; Mary P Watson; Marisa C Kozlowski
Journal:  ACS Catal       Date:  2021-06-28       Impact factor: 13.700

4.  Reductant-Free Cross-Electrophile Synthesis of Di(hetero)arylmethanes by Palladium-Catalyzed Desulfinative C-C Coupling.

Authors:  Janette McKnight; Andre Shavnya; Neal W Sach; David C Blakemore; Ian B Moses; Michael C Willis
Journal:  Angew Chem Int Ed Engl       Date:  2022-03-14       Impact factor: 16.823

5.  Lewis Basic Salt-Promoted Organosilane Coupling Reactions with Aromatic Electrophiles.

Authors:  Tyler W Reidl; Jeffrey S Bandar
Journal:  J Am Chem Soc       Date:  2021-07-27       Impact factor: 16.383

6.  Overcoming the Naphthyl Requirement in Stereospecific Cross-Couplings to Form Quaternary Stereocenters.

Authors:  Jianyu Xu; Olivia P Bercher; Mary P Watson
Journal:  J Am Chem Soc       Date:  2021-06-01       Impact factor: 16.383

  6 in total

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