Literature DB >> 34618418

First-Row d-Block Element-Catalyzed Carbon-Boron Bond Formation and Related Processes.

Shubhankar Kumar Bose1, Lujia Mao2, Laura Kuehn3, Udo Radius3, Jan Nekvinda4, Webster L Santos4, Stephen A Westcott5, Patrick G Steel6, Todd B Marder3.   

Abstract

Organoboron reagents represent a unique class of compounds because of their utility in modern synthetic organic chemistry, often affording unprecedented reactivity. The transformation of the carbon-boron bond into a carbon-X (X = C, N, and O) bond in a stereocontrolled fashion has become invaluable in medicinal chemistry, agrochemistry, and natural products chemistry as well as materials science. Over the past decade, first-row d-block transition metals have become increasingly widely used as catalysts for the formation of a carbon-boron bond, a transformation traditionally catalyzed by expensive precious metals. This recent focus on alternative transition metals has enabled growth in fundamental methods in organoboron chemistry. This review surveys the current state-of-the-art in the use of first-row d-block element-based catalysts for the formation of carbon-boron bonds.

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Year:  2021        PMID: 34618418     DOI: 10.1021/acs.chemrev.1c00255

Source DB:  PubMed          Journal:  Chem Rev        ISSN: 0009-2665            Impact factor:   60.622


  11 in total

Review 1.  Inorganometallics (Transition Metal-Metalloid Complexes) and Catalysis.

Authors:  Bogdan Marciniec; Cezary Pietraszuk; Piotr Pawluć; Hieronim Maciejewski
Journal:  Chem Rev       Date:  2021-12-30       Impact factor: 60.622

2.  NHC induced radical formation via homolytic cleavage of B-B bonds and its role in organic reactions.

Authors:  Laura Kuehn; Ludwig Zapf; Luis Werner; Martin Stang; Sabrina Würtemberger-Pietsch; Ivo Krummenacher; Holger Braunschweig; Emmanuel Lacôte; Todd B Marder; Udo Radius
Journal:  Chem Sci       Date:  2022-06-07       Impact factor: 9.969

3.  Photoinduced metal-free borylation of aryl halides catalysed by an in situ formed donor-acceptor complex.

Authors:  Manhong Li; Siqi Liu; Haoshi Bao; Qini Li; Yi-Hui Deng; Tian-Yu Sun; Leifeng Wang
Journal:  Chem Sci       Date:  2022-04-04       Impact factor: 9.969

4.  Robust dicopper(i) μ-boryl complexes supported by a dinucleating naphthyridine-based ligand.

Authors:  Pablo Ríos; Matthew S See; Rex C Handford; Simon J Teat; T Don Tilley
Journal:  Chem Sci       Date:  2022-05-13       Impact factor: 9.969

5.  Primary trifluoroborate-iminiums enable facile access to chiral α-aminoboronic acids via Ru-catalyzed asymmetric hydrogenation and simple hydrolysis of the trifluoroborate moiety.

Authors:  Andrej Šterman; Izidor Sosič; Zdenko Časar
Journal:  Chem Sci       Date:  2022-01-26       Impact factor: 9.825

6.  Catalyst-controlled selective borocarbonylation of benzylidenecyclopropanes: regiodivergent synthesis of γ-vinylboryl ketones and β-cyclopropylboryl ketones.

Authors:  Fu-Peng Wu; Xiao-Feng Wu
Journal:  Chem Sci       Date:  2022-03-21       Impact factor: 9.825

7.  Base-Mediated Radical Borylation of Alkyl Sulfones.

Authors:  Mingming Huang; Jiefeng Hu; Ivo Krummenacher; Alexandra Friedrich; Holger Braunschweig; Stephen A Westcott; Udo Radius; Todd B Marder
Journal:  Chemistry       Date:  2021-11-29       Impact factor: 5.020

8.  Dismutation of Tricyanoboryllead Compounds: The Homoleptic Tetrakis(tricyanoboryl)plumbate Tetraanion.

Authors:  Mathias Häring; Christoph Kerpen; Tatjana Ribbeck; Philipp T Hennig; Rüdiger Bertermann; Nikolai V Ignat'ev; Maik Finze
Journal:  Angew Chem Int Ed Engl       Date:  2022-04-19       Impact factor: 16.823

9.  Selective, Transition Metal-free 1,2-Diboration of Alkyl Halides, Tosylates, and Alcohols.

Authors:  Mingming Huang; Jiefeng Hu; Shasha Shi; Alexandra Friedrich; Johannes Krebs; Stephen A Westcott; Udo Radius; Todd B Marder
Journal:  Chemistry       Date:  2022-03-19       Impact factor: 5.020

10.  Copper-Catalyzed Borylation of Acyl Chlorides with an Alkoxy Diboron Reagent: A Facile Route to Acylboron Compounds.

Authors:  Xiaolei Zhang; Alexandra Friedrich; Todd B Marder
Journal:  Chemistry       Date:  2022-06-13       Impact factor: 5.020

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