Metal‐Catalyzed Multicomponent Reactions

Author(s):  
Jeffrey S. Quesnel ◽  
Bruce A. Arndtsen
Synthesis ◽  
2017 ◽  
Vol 50 (01) ◽  
pp. 1-16 ◽  
Author(s):  
Santosh Mhaske ◽  
Ranjeet Dhokale

The plethora of transformations attainable by the transition-metal-catalyzed reactions of arynes has found immense contemporary interest in the scientific community. This review highlights the scope and importance of transition-metal-catalyzed aryne reactions in the field of synthetic organic chemistry reported to date. It covers transformations achieved by the combination of arynes and various transition metals, which provide a facile access to a biaryl motif, fused polycyclic aromatic compounds, different novel carbocycles, various heterocycles, and complex natural products.1 Introduction2 Insertion of Arynes3 Annulation of Arynes4 Cycloaddition of Arynes5 Multicomponent Reactions of Arynes6 Miscellaneous Reactions of Arynes7 Total Synthesis of Natural Products Using Arynes8 Conclusion


2019 ◽  
Vol 4 (1) ◽  
pp. 100-104 ◽  
Author(s):  
Saeed Bahadorikhalili ◽  
Golnaz Rahimzadeh ◽  
Ebrahim Kianmehr ◽  
Samira Ansari ◽  
Haleh Hamedifar ◽  
...  

ChemInform ◽  
2008 ◽  
Vol 39 (3) ◽  
Author(s):  
Genevieve Balme ◽  
Didier Bouyssi ◽  
Nuno Monteiro

2017 ◽  
Vol 15 (43) ◽  
pp. 9031-9043 ◽  
Author(s):  
Jie-Ping Wan ◽  
Lu Gan ◽  
Yunyun Liu

Research advances in transition metal-catalyzed multicomponent C–H functionalization reactions over the last decade are summarized.


2005 ◽  
pp. 224-276 ◽  
Author(s):  
Geneviève Balme ◽  
Didier Bouyssi ◽  
Nuno Monteiro

Synthesis ◽  
2021 ◽  
Author(s):  
Tom G. Driver ◽  
Wrickban Mazumdar

AbstractRecent catalytic methods to construct medium-sized lactams­ and partially saturated benzazepines and their derivatives are surveyed. The review is divided into the following sections:1 Introduction2 Non-Transition-Metal-Catalyzed Reactions2.1 Beckmann Rearrangement2.2 Non-Beckmann Rearrangement Reactions2.3 Multicomponent reactions3 Transition-Metal-Catalyzed Reactions3.1 Gold-Catalyzed Reactions to Access Medium-Sized N-Hetero­cycles3.2 Reactions Involving a Metal η3-Complex Catalytic Intermediate3.3 Transition-Metal-Catalyzed Reactions of Strained Cycloalkanes4 Conclusions


Synlett ◽  
2020 ◽  
Vol 31 (08) ◽  
pp. 750-771
Author(s):  
Daesung Lee ◽  
Sourav Ghorai

Multicomponent reactions (MCRs) constitute a powerful synthetic tool to generate a large number of small molecules with high atom economy, which thus can efficiently expand the chemical space with molecular diversity and complexity. Aryne-based MCRs offer versatile possibilities to construct functionalized arenes and benzo-fused heterocycles. Because of their electrophilic nature, arynes couple with a broad range of nucleophiles. Thus, a variety of aryne-based MCRs have been developed, the representative of which are summarized in this account.1 Introduction2 Aryne-Based Multicomponent Reactions2.1 Trapping with Isocyanides2.2 Trapping with Imines2.3 Trapping with Amines2.4 Insertion into π-Bonds2.5 Trapping with Ethers and Thioethers2.6 Trapping with Carbanions2.7 Transition-Metal-Catalyzed Approaches3 Strategies Based on Hexadehydro Diels–Alder Reaction3.1 Dihalogenation3.2 Halohydroxylation and Haloacylation3.3 Amides and Imides3.4 Quinazolines3.5 Benzocyclobutene-1,2-diimines and 3H-Indole-3-imines3.6 Other MCRs of Arynes and Isocyanides4 Conclusion


Synthesis ◽  
2017 ◽  
Vol 28 (19) ◽  
pp. 4414-4433 ◽  
Author(s):  
Xuefeng Jiang ◽  
Minghao Feng

Arynes are important building blocks for introducing aromatic rings into molecules and they are frequently utilized in syntheses. Historically, arynes were generated under harsh conditions and this limited their use. Arynes can now be generated under milder conditions, e.g. from 2-(trimethylsilyl)phenyl triflate, and utilized in transition-metal­ catalyzed reactions such as [2+2+2] reactions, insertion into σ-bonds, cascade cyclizations and C–H activation reactions. This short review focuses on transition-metal-catalyzed reactions relevant to aryne intermediates generated from 2-(trimethylsilyl)phenyl triflates and other aryne precursors.1 Introduction2 [2+2+2] Reactions3 Aryne Insertion into a σ-Bond4 Cascade Cyclizations5 C–H Activation6 Multicomponent Reactions (MCRs)7 Conclusion


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