Literature DB >> 32486635

Sulfonate Versus Sulfonate: Nickel and Palladium Multimetallic Cross-Electrophile Coupling of Aryl Triflates with Aryl Tosylates.

Kai Kang1, Liangbin Huang2, Daniel J Weix1.   

Abstract

While phenols are frequent and convenient aryl sources in cross-coupling, typically as sulfonate esters, the direct cross-Ullmann coupling of two different sulfonate esters is unknown. We report here a general solution to this challenge catalyzed by a combination of Ni and Pd with Zn reductant and LiBr as an additive. The reaction has broad scope, as demonstrated in 33 examples (65% ± 11% average yield). Mechanistic studies show that Pd strongly prefers the aryl triflate, the Ni catalyst has a small preference for the aryl tosylate, aryl transfer between catalysts is mediated by Zn, and Pd improves yields by consuming arylzinc intermediates.

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Year:  2020        PMID: 32486635      PMCID: PMC7373434          DOI: 10.1021/jacs.0c04670

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  56 in total

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Authors:  Brad M Rosen; Kyle W Quasdorf; Daniella A Wilson; Na Zhang; Ana-Maria Resmerita; Neil K Garg; Virgil Percec
Journal:  Chem Rev       Date:  2010-12-06       Impact factor: 60.622

2.  Palladium-catalyzed borylation of aryl mesylates and tosylates and their applications in one-pot sequential Suzuki-Miyaura biaryl synthesis.

Authors:  Wing Kin Chow; Chau Ming So; Chak Po Lau; Fuk Yee Kwong
Journal:  Chemistry       Date:  2011-05-05       Impact factor: 5.236

3.  Cobalt-catalyzed cross-coupling reactions.

Authors:  Gérard Cahiez; Alban Moyeux
Journal:  Chem Rev       Date:  2010-03-10       Impact factor: 60.622

Review 4.  Large-scale applications of transition metal-catalyzed couplings for the synthesis of pharmaceuticals.

Authors:  Javier Magano; Joshua R Dunetz
Journal:  Chem Rev       Date:  2011-03-09       Impact factor: 60.622

5.  A Pd-catalyzed, boron ester-mediated, reductive cross-coupling of two aryl halides to synthesize tricyclic biaryls.

Authors:  Zhilong Chen; Xiaodong Wang
Journal:  Org Biomol Chem       Date:  2017-06-29       Impact factor: 3.876

6.  Copper-catalysed cross-coupling: an untapped potential.

Authors:  Surendra Thapa; Bijay Shrestha; Santosh K Gurung; Ramesh Giri
Journal:  Org Biomol Chem       Date:  2015-05-07       Impact factor: 3.876

7.  Identification of a higher-order organozincate intermediate involved in Negishi cross-coupling reactions by mass spectrometry and NMR spectroscopy.

Authors:  Howard N Hunter; Niloufar Hadei; Voislav Blagojevic; Pascal Patschinski; George T Achonduh; Stephanie Avola; Diethard K Bohme; Michael G Organ
Journal:  Chemistry       Date:  2011-06-08       Impact factor: 5.236

Review 8.  Polyphenols: chemistry, dietary sources, metabolism, and nutritional significance.

Authors:  L Bravo
Journal:  Nutr Rev       Date:  1998-11       Impact factor: 7.110

9.  Neopentylglycolborylation of aryl mesylates and tosylates catalyzed by Ni-based mixed-ligand systems activated with Zn.

Authors:  Daniela A Wilson; Christopher J Wilson; Costel Moldoveanu; Ana-Maria Resmerita; Patrick Corcoran; Lisa M Hoang; Brad M Rosen; Virgil Percec
Journal:  J Am Chem Soc       Date:  2010-02-17       Impact factor: 15.419

10.  Selective ortho-Functionalization of Adamantylarenes Enabled by Dispersion and an Air-Stable Palladium(I) Dimer.

Authors:  Indrek Kalvet; Kristina Deckers; Ignacio Funes-Ardoiz; Guillaume Magnin; Theresa Sperger; Marius Kremer; Franziska Schoenebeck
Journal:  Angew Chem Int Ed Engl       Date:  2020-03-17       Impact factor: 15.336

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  5 in total

1.  A General, Multimetallic Cross-Ullmann Biheteroaryl Synthesis from Heteroaryl Halides and Heteroaryl Triflates.

Authors:  Kai Kang; Nathan L Loud; Tarah A DiBenedetto; Daniel J Weix
Journal:  J Am Chem Soc       Date:  2021-12-17       Impact factor: 15.419

2.  Zirconium-Redox-Shuttled Cross-Electrophile Coupling of Aromatic and Heteroaromatic Halides.

Authors:  Ting-Feng Wu; Yue-Jiao Zhang; Yue Fu; Fang-Jie Liu; Jian-Tao Tang; Peng Liu; F Dean Toste; Baihua Ye
Journal:  Chem       Date:  2021-07-08       Impact factor: 25.832

3.  Nickel Catalyzed Vinylidene Insertions into O-H Bonds.

Authors:  Houng Kang; Christopher Uyeda
Journal:  ACS Catal       Date:  2020-12-15       Impact factor: 13.084

4.  Nickel-catalyzed cross-electrophile allylation of vinyl bromides and the modification of anti-tumour natural medicine β-elemene.

Authors:  Yang Ye; Xiang Qi; Bing Xu; Ying Lin; Huan Xiang; Liang Zou; Xiang-Yang Ye; Tian Xie
Journal:  Chem Sci       Date:  2022-05-12       Impact factor: 9.969

5.  Ruthenium catalyzed β-selective alkylation of vinylpyridines with aldehydes/ketones via N2H4 mediated deoxygenative couplings.

Authors:  Leiyang Lv; Chao-Jun Li
Journal:  Chem Sci       Date:  2020-12-30       Impact factor: 9.825

  5 in total

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