Sigma-Bond Metathesis as an Unusual Asymmetric Induction Step in Rhodium-Catalyzed Enantiodivergent Synthesis of C–N Axially Chiral Biaryls DOI
Peiyuan Wang, Hongli Wu, Xuepeng Zhang

и другие.

Journal of the American Chemical Society, Год журнала: 2023, Номер 145(15), С. 8417 - 8429

Опубликована: Март 23, 2023

Mechanistic understanding of asymmetric induction plays a crucial role in designing new catalytic reactions. Reported herein is atroposelective access to C-N axially chiral isoquinolones via rhodium-catalyzed C-H activation N-alkoxy benzamides and annulation with imidoyl sulfoxonium ylides. The coupling system proceeded excellent functional group tolerance, different conditions were identified afford one or the other enantiomeric product each enantioselectivity for representative class ylide reagent, thus making both enantiomers readily available using same catalyst. Experimental computational studies revealed pathway alkylation enantio-determining formal nucleophilic substitution-C-N cyclization that mediated by rhodium catalyst σ-bond metathesis as mechanism. Computational indicated solvent-dependent enatiodivergence originated from levels neutral versus cationic species.

Язык: Английский

A comprehensive overview of directing groups applied in metal-catalysed C–H functionalisation chemistry DOI Creative Commons
Carlo Sambiagio, David Schönbauer, Rémi Blieck

и другие.

Chemical Society Reviews, Год журнала: 2018, Номер 47(17), С. 6603 - 6743

Опубликована: Янв. 1, 2018

The present review is devoted to summarizing the recent advances (2015-2017) in field of metal-catalysed group-directed C-H functionalisation. In order clearly showcase molecular diversity that can now be accessed by means directed functionalisation, whole organized following directing groups installed on a substrate. Its aim comprehensive reference work, where specific group easily found, together with transformations which have been carried out it. Hence, primary format this schemes accompanied concise explanatory text, are ordered sections according their chemical structure. feature typical substrates used, products obtained as well required reaction conditions. Importantly, each example commented respect most important positive features and drawbacks, aspects such selectivity, substrate scope, conditions, removal, greenness. targeted readership both experts functionalisation chemistry (to provide overview progress made last years) and, even more so, all organic chemists who want introduce way thinking for design straightforward, efficient step-economic synthetic routes towards molecules interest them. Accordingly, should particular also scientists from industrial R&D sector. overall goal promote application reactions outside research dedicated method development establishing it valuable archetype contemporary R&D, comparable role cross-coupling play date.

Язык: Английский

Процитировано

1464

Bond-Forming and -Breaking Reactions at Sulfur(IV): Sulfoxides, Sulfonium Salts, Sulfur Ylides, and Sulfinate Salts DOI Creative Commons
Daniel Kaiser, Immo Klose,

Rik Oost

и другие.

Chemical Reviews, Год журнала: 2019, Номер 119(14), С. 8701 - 8780

Опубликована: Июнь 25, 2019

Organosulfur compounds have long played a vital role in organic chemistry and the development of novel chemical structures architectures. Prominent among these organosulfur are those involving sulfur(IV) center, which been subject countless investigations over more than hundred years. In addition to list textbook sulfur-based reactions, there has sustained interest organosulfur(IV) recent Of particular within is ease with synthetic chemist can effect wide range transformations through either bond formation or cleavage at sulfur. This review aims cover developments past decade molecules provide insight into both reactions critically rely on this versatile element diverse scaffolds that thereby be synthesized.

Язык: Английский

Процитировано

698

Rhodium(iii)-catalyzed chemodivergent annulations between N-methoxybenzamides and sulfoxonium ylides via C–H activation DOI
Youwei Xu, Guangfan Zheng, Xifa Yang

и другие.

Chemical Communications, Год журнала: 2018, Номер 54(6), С. 670 - 673

Опубликована: Янв. 1, 2018

Rhodium-catalyzed and acid-controlled chemodivergent annulations between N-methoxybenzamides sulfoxonium ylides have been realized.

Язык: Английский

Процитировано

189

Rhodium(iii)-catalyzed annulative coupling between arenes and sulfoxonium ylides via C–H activation DOI
Guangfan Zheng, Miaomiao Tian, Youwei Xu

и другие.

Organic Chemistry Frontiers, Год журнала: 2017, Номер 5(6), С. 998 - 1002

Опубликована: Дек. 22, 2017

Sulfoxonium ylides acts as a bifunctional C2-synthon in Rh(iii)-catalyzed redox-neutral annulative coupling with arenes for the synthesis of N-heterocycles and carbocycles.

Язык: Английский

Процитировано

153

Rhodium-Catalyzed Relay Carbenoid Functionalization of Aromatic C–H Bonds toward Fused Heteroarenes DOI
Xiaopeng Wu, Hao Xiong, Song Sun

и другие.

Organic Letters, Год журнала: 2018, Номер 20(5), С. 1396 - 1399

Опубликована: Фев. 22, 2018

A rhodium-catalyzed annulation between ethyl benzimidates and α- aroyl sulfur ylides was developed, affording a series of pyrano[4,3,2-ij]isoquinoline derivatives in moderate to good yields with functional group compatibility. The procedure featured dual ortho-C–H functionalization cyclization one pot. optoelectronic properties those fused heteroarenes were tested by UV/vis fluorescence spectrometers.

Язык: Английский

Процитировано

142

Rh(III)-Catalyzed Cascade Reactions of Sulfoxonium Ylides with α-Diazocarbonyl Compounds: An Access to Highly Functionalized Naphthalenones DOI
Xi Chen, Muhua Wang, Xinying Zhang

и другие.

Organic Letters, Год журнала: 2019, Номер 21(8), С. 2541 - 2545

Опубликована: Апрель 8, 2019

An unprecedented cascade reaction of benzoyl sulfoxonium ylides with α-diazocarbonyl compounds leading to the formation highly functionalized naphthalenones containing a β-ketosulfoxonium ylide moiety is presented. Promisingly, naphthalenone derivative thus obtained was found be versatile intermediate toward diversely naphthalene derivatives including substituted 1-naphthol, 2-hydroxynaphthalen-1(2H)-one, naphthalen-1,2-dione, and 2-(methylsulfinyl)naphthalen-1-ol.

Язык: Английский

Процитировано

133

Sulfur-Based Ylides in Transition-Metal-Catalysed Processes DOI Creative Commons
James D. Neuhaus,

Rik Oost,

Jérémy Merad

и другие.

Topics in Current Chemistry, Год журнала: 2018, Номер 376(3)

Опубликована: Апрель 13, 2018

Traditionally employed in the synthesis of small ring systems and rearrangement chemistry, sulfur-based ylides occupy a unique position toolbox synthetic organic chemist. In recent years number pioneering researchers have looked to expand application these unorthodox reagents through use transition metal catalysis. The strength flexibility such combination been shown be key importance developing powerful novel methodologies. This chapter summarises developments metal-catalysed sulfonium/sulfoxonium ylide reactions, as well providing historical perspective. overviewing successes this area, authors hope encourage others into growing field.

Язык: Английский

Процитировано

131

Selective Synthesis of Benzo[a]Carbazoles and Indolo[2,1‐a]‐Isoquinolines via Rh(III)‐Catalyzed C−H Functionalizations of 2‐Arylindoles with Sulfoxonium Ylides DOI
Guang Chen, Xinying Zhang,

Ruixue Jia

и другие.

Advanced Synthesis & Catalysis, Год журнала: 2018, Номер 360(19), С. 3781 - 3787

Опубликована: Июль 12, 2018

Abstract A highly chem‐ and regioselective synthesis of diversely substituted benzo[ a ]carbazoles indolo[2,1‐ ]‐isoquinolines through Rh(III)‐catalyzed cascade reactions 2‐arylindoles with sulfoxonium ylides is presented. To be specific, treatment 2‐arylindoles, 2‐arylindole‐3‐carbaldehydes, 2‐arylindole‐3‐carbonitriles or 2‐aryl‐3‐methylindoles under the catalysis Rh(III) led to selective formation 6‐aryl/alkyl ]carbazoles, 5‐acylbenzo[ 6‐amino‐5‐acylbenzo[ 12‐methylindolo[2,1‐ ]isoquinolines, respectively. Mechanistically, title compounds involves process including metalation inert C( sp 2 )−H bond, migratory insertion ylide into carbon‐metal bond via an in situ carbenoid formation, protodemetalation, condensation. our knowledge, this first example which β‐carbonyl were used as stable carbene precursors bifunctional C2 synthons afford ]isoquinolines. magnified image

Язык: Английский

Процитировано

124

Beyond Friedel and Crafts: Directed Alkylation of C−H Bonds in Arenes DOI
Gwilherm Evano, Cédric Theunissen

Angewandte Chemie International Edition, Год журнала: 2018, Номер 58(22), С. 7202 - 7236

Опубликована: Авг. 14, 2018

Abstract Alkylation of arenes is one the most fundamental transformations in chemical synthesis and leads to privileged scaffolds many areas science. Classical methods for introduction alkyl groups are mostly based on Friedel–Crafts reaction, radical additions, metalation, or prefunctionalization arene: these methods, however, suffer from limitations scope, efficiency, selectivity. Moreover, they innate reactivity starting arene, favoring alkylation at a certain position rendering chains other positions much more challenging. This can be addressed by use directing group that facilitates, presence metal catalyst, regioselective C−H bond. These directed alkylations bonds will comprehensively summarized this Review.

Язык: Английский

Процитировано

124

Cp*M-Catalyzed Direct Annulation with Terminal Alkynes and Their Surrogates for the Construction of Multi-Ring Systems DOI
Yuji Nishii, Masahiro Miura

ACS Catalysis, Год журнала: 2020, Номер 10(17), С. 9747 - 9757

Опубликована: Авг. 3, 2020

Transition-metal-catalyzed C–H activation followed by oxidative cyclization with unsaturated coupling partners has been a valuable synthetic tool for the multiring molecular scaffolds. This Perspective introduces recent progress on Cp*M-catalyzed (M = Co, Rh, and Ir) direct annulation of functionalized arenes terminal alkynes their equivalents through bond cleavage. The highlighted examples are categorized according to 10 different types reagents used in transformations. representative conditions, selected reaction scope, key mechanistic aspects briefly summarized.

Язык: Английский

Процитировано

122