Literature DB >> 30525176

Metal-catalyzed cross-coupling chemistry with polyhedral boranes.

Rafal M Dziedzic1, Alexander M Spokoyny.   

Abstract

Over the past several decades, metal-catalyzed cross-coupling has emerged as a very powerful strategy to functionalize carbon-based molecules. More recently, some of the cross-coupling methodologies have been adapted to inorganic compounds including boron-rich clusters. The development of this chemistry relies on the ability to synthesize halogenated boron-rich clusters which can serve as electrophilic cross-coupling partners with nucleophilic substrates in the presence of a metal catalyst. While the cross-coupling chemistry with boron-clusters is conceptually reminiscent of that of its hydrocarbon counterparts, several key aspects including the spheroidal bulk of clusters and the distinct nature of boron-halogen/boron-heteroatom bonds make this chemistry unique. The utility of metal-catalyzed cross-coupling can be extended to several classes of polyhedral boranes including neutral and anionic carboranes, metallaboranes, and carbon-free boranes. Importantly, cross-coupling enables a suite of boron-heteroatom (C, N, O, P, S) couplings to prepare boron cluster-based systems that can be used for ligand design, medicinal chemistry, and materials applications.

Entities:  

Year:  2019        PMID: 30525176      PMCID: PMC6491218          DOI: 10.1039/c8cc08693a

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  55 in total

1.  Methylation of Boron Vertices of the Cobalt Dicarbollide Anion.

Authors:  Mark D. Mortimer; Carolyn B. Knobler; M. Frederick Hawthorne
Journal:  Inorg Chem       Date:  1996-09-11       Impact factor: 5.165

2.  Relevance of the electronegativity of boron in eta5-coordinating ligands: regioselective monoalkylation and monoarylation in cobaltabisdicarbollide [3,3'-Co(1,2-C2B9H11)2]- clusters.

Authors:  Isabel Rojo; Francesc Teixidor; Clara Viñas; Raikko Kivekäs; Reijo Sillanpää
Journal:  Chemistry       Date:  2003-09-22       Impact factor: 5.236

3.  Three-dimensional aromaticity in polyhedral boranes and related molecules.

Authors:  R B King
Journal:  Chem Rev       Date:  2001-05       Impact factor: 60.622

4.  Synthesis and structural characterization of highly chlorinated, brominated, iodinated, and methylated carborane anions, 1-H-CB9X9-, 1-NH2-CB9X9- (X = Cl, Br, I), and 1-H-CB9(CH3)9-.

Authors:  C W Tsang; Q Yang; E T Sze; T C Mak; D T Chan; Z Xie
Journal:  Inorg Chem       Date:  2000 Aug, 7       Impact factor: 5.165

5.  Synthesis of a Metallaborane Complex Containing Pd(III) and the First Doubly Charge Compensated Ollide Ion. X-ray Crystal Structure of 1,4-Br(2)-1,2,5-(PMe(2)Ph)(3)-closo-1-PdB(11)H(8).

Authors:  Steve A. Jasper; John C. Huffman; Lee J. Todd
Journal:  Inorg Chem       Date:  1998-11-16       Impact factor: 5.165

6.  Palladium-catalyzed Heck reactions of styrene derivatives and 2-iodo-p-carborane.

Authors:  Ludvig Eriksson; Karl Johan Winberg; Rodrigo Tascon Claro; Stefan Sjöberg
Journal:  J Org Chem       Date:  2003-05-02       Impact factor: 4.354

7.  Structural characterization of cationic liposomes loaded with sugar-based carboranes.

Authors:  Sandra Ristori; Julian Oberdisse; Isabelle Grillo; Alessandro Donati; Olivier Spalla
Journal:  Biophys J       Date:  2004-10-15       Impact factor: 4.033

8.  Synthesis of mono- and dihalogenated derivatives of (Me2S)2B12H10 and palladium-catalyzed boron-carbon cross-coupling reactions of the iodides with grignard reagents.

Authors:  Roman G Kultyshev; Shengming Liu; Hoitung T Leung; Jianping Liu; Sheldon G Shore
Journal:  Inorg Chem       Date:  2003-05-19       Impact factor: 5.165

9.  Mercuracarborand "anti-crown ether"-based chloride-sensitive liquid/polymeric membrane electrodes.

Authors:  I H Badr; M Diaz; M F Hawthorne; L G Bachas
Journal:  Anal Chem       Date:  1999-04-01       Impact factor: 6.986

10.  Formation of bridging alkene and conjugated dialkenes exclusively generated from alkynes on the [3,3'-Co(1,2-C2B9H11)2]- platform. The unique hydroboration role of [3,3'-Co(1,2-C2B9H11)2]-.

Authors:  Isabel Rojo; Francesc Teixidor; Raikko Kivekäs; Reijo Sillanpää; Clara Viñas
Journal:  J Am Chem Soc       Date:  2003-12-03       Impact factor: 15.419

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  9 in total

1.  Oxidative Generation of Boron-Centered Radicals in Carboranes.

Authors:  Harrison A Mills; Joshua L Martin; Arnold L Rheingold; Alexander M Spokoyny
Journal:  J Am Chem Soc       Date:  2020-03-03       Impact factor: 15.419

2.  Off-Cycle Processes in Pd-Catalyzed Cross-Coupling of Carboranes.

Authors:  Rafal M Dziedzic; Jonathan C Axtell; Arnold L Rheingold; Alexander M Spokoyny
Journal:  Org Process Res Dev       Date:  2019-08-05       Impact factor: 3.317

Review 3.  Carboranes as unique pharmacophores in antitumor medicinal chemistry.

Authors:  Yu Chen; Fukuan Du; Liyao Tang; Jinrun Xu; Yueshui Zhao; Xu Wu; Mingxing Li; Jing Shen; Qinglian Wen; Chi Hin Cho; Zhangang Xiao
Journal:  Mol Ther Oncolytics       Date:  2022-01-10       Impact factor: 7.200

4.  Ir-catalyzed enantioselective B-H alkenylation for asymmetric synthesis of chiral-at-cage o‑carboranes.

Authors:  Ruofei Cheng; Jie Zhang; Huifang Zhang; Zaozao Qiu; Zuowei Xie
Journal:  Nat Commun       Date:  2021-12-08       Impact factor: 14.919

Review 5.  Electrochemical Cage Activation of Carboranes.

Authors:  Long Yang; Zi-Jing Zhang; Becky Bongsuiru Jei; Lutz Ackermann
Journal:  Angew Chem Int Ed Engl       Date:  2022-03-25       Impact factor: 16.823

6.  Magnesium-mediated sp3 C-H activation in cascade cyclization of 1-arylethynyl-2-alkyl-o-carboranes: efficient synthesis of carborane-fused cyclopentanes.

Authors:  Jie Zhang; Cen Tang; Zuowei Xie
Journal:  Chem Sci       Date:  2020-09-02       Impact factor: 9.825

7.  Tri-insertion with dearomatization of terminal arylalkynes using a carborane based frustrated Lewis pair template.

Authors:  Jian Zhang; Zuowei Xie
Journal:  Chem Sci       Date:  2020-11-28       Impact factor: 9.825

8.  Electrochemical B-H Nitrogenation: Access to Amino Acid and BODIPY-Labeled nido-Carboranes.

Authors:  Long Yang; Becky Bongsuiru Jei; Alexej Scheremetjew; Rositha Kuniyil; Lutz Ackermann
Journal:  Angew Chem Int Ed Engl       Date:  2020-11-17       Impact factor: 15.336

9.  Regioselective B(3,4)-H arylation of o-carboranes by weak amide coordination at room temperature.

Authors:  Yu-Feng Liang; Long Yang; Becky Bongsuiru Jei; Rositha Kuniyil; Lutz Ackermann
Journal:  Chem Sci       Date:  2020-05-05       Impact factor: 9.825

  9 in total

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