Iridium-Catalyzed Regioselective B(4)-Alkenylation and B(3,5)-Dialkenylation of o-Carboranes DOI
Hee Chan Noh, Cheol‐Eui Kim, Kyungsup Lee

и другие.

Organic Letters, Год журнала: 2023, Номер 25(36), С. 6643 - 6648

Опубликована: Авг. 30, 2023

Iridium(I)-catalyzed regioselective B(4)-alkenylation has been developed from o-carboranyl sulfoxonium ylides and alkynes through B(4)–H activation. The sequential B(4)- B(6)-alkenylation afforded B(3,5)-dialkenylated in one pot. Eventually, two alkenyl groups, the same or different, were introduced at positions 3 5 of carborane. Sulfoxonium ylide used as a directing group remains available for further functionalization is converted to B-alkenylated trichloromethyl ketones.

Язык: Английский

The transition metal-catalysed hydroboration reaction DOI Creative Commons
Stephen J. Geier, Christopher M. Vogels, Jennifer A. Melanson

и другие.

Chemical Society Reviews, Год журнала: 2022, Номер 51(21), С. 8877 - 8922

Опубликована: Янв. 1, 2022

This review covers the development of transition metal-catalysed hydroboration reaction, from its beginnings in 1980s to more recent developments including earth-abundant catalysts and an ever-expanding array substrates.

Язык: Английский

Процитировано

150

A Strategy for Selective Catalytic B–H Functionalization of o-Carboranes DOI
Zaozao Qiu, Zuowei Xie

Accounts of Chemical Research, Год журнала: 2021, Номер 54(21), С. 4065 - 4079

Опубликована: Окт. 24, 2021

ConspectusCarboranes are a class of polyhedral carbon-boron molecular clusters featuring three-dimensional aromaticity, which often considered as 3D analogues benzene. Their unique structural and electronic properties make them invaluable building blocks for applications ranging from functional materials to versatile ligands pharmaceuticals. Thus, selective functionalization carboranes has received tremendous research interest. In earlier days, the vast majority works in this area were focused on cage carbon via facile deprotonation CH, followed by reaction with electrophiles. On contrary, B-H activation is very challenging since 10 bonds o-carborane similar, how achieve desired transformation at specific boron vertex long-standing issue.As more electronegative than boron, property results different charges cage, follow order B(3,6)-H ≪ B(4,5,7,11)-H < B(8,10)-H B(9,12)-H. We thought that difference may trigger favorite interaction proper transition metal complex bond carborane, could be utilized solve selectivity issue. Accordingly, our strategy described follows: (1) electron-rich catalysts good most electron-deficient (connected both C-H vertices); (2) relatively B(8,9,10,12)-H (with no bonding either (3) directing-group-assisted catalysis appropriate only one vertex), whose lie middle range bonds. This been successfully applied laboratory other groups development series synthetic routes catalytic carborane resulting synthesis large number cage-boron-functionalized derivatives regioselective fashion. Subsequently, significant progress emerging made.In 2013 we reported tetrafluorination o-carboranes using an Pd(II) salt, [Pd(MeCN)4][BF4], catalyst. 2014 disclosed first example carboxy-directed alkenylation B(4) promoted Ir(III) 2017 presented Ir(I)-catalyzed diborylation also uncovered Pd-catalyzed asymmetric chiral-at-cage 2018. These proof-of-principle studies have greatly stimulated activities enabled catalysts. so far developed toolbox methods B-olefination, -arylation, -alkenylation, -alkynylation, -oxygenation, -sulfenylation, -borylation, -halogenation, -amination. recently expanded base catalysis. As field progresses, expect will invented, detailed Account promote these efforts.

Язык: Английский

Процитировано

114

Recent Advances in Transition Metal-Catalyzed Selective B-H Functionalization ofo-Carboranes DOI Open Access
Yik Ki Au, Zuowei Xie

Bulletin of the Chemical Society of Japan, Год журнала: 2020, Номер 94(3), С. 879 - 899

Опубликована: Дек. 18, 2020

Abstract Carboranes are a class of carbon-boron molecular clusters, possessing extraordinary characteristics including three-dimensional aromaticity conjugated by σ-bonds, icosahedral geometry and inherent robustness. They finding growing applications as valuable building blocks in boron neutron capture therapy agents, pharmacophores, nanomaterials, optoelectronic, organometallic/coordination chemistry more. Therefore, the effective controlled functionalization carboranes has attracted enormous research interests, particularly regio- enantio-selective cage BH derivatization among ten chemically similar vertices o-carboranes. Only recent few years, significant progress been made transition metal catalyzed vertex-specific functionalization. This review summarizes advances this realm.

Язык: Английский

Процитировано

78

Copper-Catalyzed Electrochemical Selective B–H Oxygenation of o-Carboranes at Room Temperature DOI
Yik Ki Au, Hairong Lyu, Yangjian Quan

и другие.

Journal of the American Chemical Society, Год журнала: 2020, Номер 142(15), С. 6940 - 6945

Опубликована: Март 31, 2020

Copper-catalyzed electrochemical selective cage B–H oxygenation of o-carboranes has been achieved for the first time. Under a constant electric current (4.0 mA) at room temperature, copper-catalyzed cross-coupling carboranyl amides with lithium phenolates results in formation B(4,5)-diphenolated via direct activation, whereas use tert-butoxide affords B(4)-monooxygenated products. This reaction does not require any additional chemical oxidants and generates H2 salt as byproducts. Control experiments indicated that high-valent Cu(III) species is likely involved process.

Язык: Английский

Процитировано

62

Regioselective B(3,4)–H arylation of o-carboranes by weak amide coordination at room temperature DOI Creative Commons
Yu‐Feng Liang, Long Yang,

Becky Bongsuiru Jei

и другие.

Chemical Science, Год журнала: 2020, Номер 11(39), С. 10764 - 10769

Опубликована: Янв. 1, 2020

B–H: site-selective B(3,4)–H arylations were accomplished at room temperature by versatile palladium catalysis enabled weakly coordinating amides.

Язык: Английский

Процитировано

56

Ir-Catalyzed Selective B(3)-H Amination of o-Carboranes with NH3 DOI
Yik Ki Au, Jie Zhang, Yangjian Quan

и другие.

Journal of the American Chemical Society, Год журнала: 2021, Номер 143(11), С. 4148 - 4153

Опубликована: Март 15, 2021

Ammonia gas, NH3, is a cheap and widely used industrial feedstock, which has received tremendous research interests in its functionalization. This work reports breakthrough catalytic selective cage B(3)-H amination of o-carboranes with NH3 via Ir-catalyzed B-H/N-H dehydrocoupling, offering convenient efficient access to series 3-NH2-o-carborane derivatives moderate high isolated yields broad substrate scope. The employment readily available gas as the aminating reagent H2 sole byproduct endows protocol economy, practicability, environmental friendliness. A plausible reaction mechanism proposed on basis control experiments.

Язык: Английский

Процитировано

47

8-Aminoquinoline as a bidentate traceless directing group for Cu-catalyzed selective B(4,5)–H disulfenylation ofo-carboranes DOI
Yu Chen, Yangjian Quan, Zuowei Xie

и другие.

Chemical Communications, Год журнала: 2020, Номер 56(85), С. 12997 - 13000

Опубликована: Янв. 1, 2020

A traceless bidentate directing group guided copper catalyzed direct cage B(4,5)-H disulfenylation of o-carboranes has been achieved, leading to a series B(4,5)-disulfenylated o-carborane derivatives in high yields with excellent regioselectivity. The situ departure the 8-aminoquinoline auxiliary circumvents additional processes for removal, thus enhancing atom-/step-economy.

Язык: Английский

Процитировано

34

Looking deep into C–H functionalization: the synthesis and application of cyclopentadienyl and related metal catalysts DOI
Guilherme A. M. Jardim, Renato L. Carvalho, Mateus P. Nunes

и другие.

Chemical Communications, Год журнала: 2022, Номер 58(19), С. 3101 - 3121

Опубликована: Янв. 1, 2022

This feature review is focused on recent key applications of commonly used transition-metal Cp-type catalysts for C–H bond functionalizations.

Язык: Английский

Процитировано

23

Palladium Catalyzed Selective B(3)–H Activation/Oxidative Dehydrogenative Coupling for the Synthesis of Bis(o-carborane)s DOI

Ji Wu,

Ke Cao, Caiyan Zhang

и другие.

Inorganic Chemistry, Год журнала: 2020, Номер 59(23), С. 17340 - 17346

Опубликована: Ноя. 24, 2020

A palladium catalyzed selective B(3)-H activation/oxidative dehydrogenative coupling for the synthesis of bis(o-carborane)s connected with B(3)-B(3') and B(3)-B(6') bonds has been developed first time. plausible mechanism involving stepwise activation B(3'/6')-H by PdII PdIV was proposed. This work is example most efficient protocol bonds, which important reference design, synthesis, application in related fields.

Язык: Английский

Процитировано

32

Catalytic Cage BH Functionalization of Carboranes via “Cage Walking” Strategy DOI

Chenyang Guo,

Zaozao Qiu, Zuowei Xie

и другие.

ACS Catalysis, Год журнала: 2021, Номер 11(4), С. 2134 - 2140

Опубликована: Фев. 3, 2021

Carboranes, three-dimensional analogues of benzene, are finding a wide variety applications ranging from functional materials to pharmaceuticals, which has drawn tremendous research interest. The recent development transition-metal-catalyzed cage B–H functionalization can realize series vertex-specific carboranes, the "cage-walking" strategy provide BH at different positions where initial bond activation occurs achieve functionalized carboranes that difficult access by conventional methods. In this Viewpoint, we will discuss concept cage-walking and its application in selective highlighting typical examples, could some valuable insights into future carborane multifunctionalization.

Язык: Английский

Процитировано

26