Synergistic Cooperative Effect of Sodium borohydride-Iodine Towards Cascade C−N and C−S/Se Bond Formation: One-pot Regioselective Synthesis of 3-Sulfenyl/selenyl Indoles and Mechanistic Insight

2017 ◽  
Vol 360 (1) ◽  
pp. 180-185 ◽  
Author(s):  
Aditya G. Lavekar ◽  
Danish Equbal ◽  
Saima ◽  
Arun K. Sinha
Keyword(s):  
Sodium Borohydride ◽  
Bond Formation ◽  
Cooperative Effect ◽  
Regioselective Synthesis ◽  
One Pot ◽  
Mechanistic Insight

Copper-Catalyzed C–O Bond Formation: An Efficient One-Pot Highly Regioselective Synthesis of Furans from (2-Furyl)Carbene Complexes

2013 ◽  
Vol 15 (5) ◽  
pp. 1080-1083 ◽  
Author(s):  
Hua Cao ◽  
Haiying Zhan ◽  
Jinghe Cen ◽  
Jingxin Lin ◽  
Yuanguang Lin ◽  
...  
Keyword(s):  
Bond Formation ◽  
Regioselective Synthesis ◽  
One Pot ◽  
Carbene Complexes

ChemInform Abstract: Copper-Catalyzed C-O Bond Formation: An Efficient One-Pot Highly Regioselective Synthesis of Furans from (2-Furyl)carbene Complexes.

ChemInform ◽  
2013 ◽  
Vol 44 (26) ◽  
pp. no-no
Author(s):  
Hua Cao ◽  
Haiying Zhan ◽  
Jinghe Cen ◽  
Jingxin Lin ◽  
Yuanguang Lin ◽  
...  
Keyword(s):  
Bond Formation ◽  
Regioselective Synthesis ◽  
One Pot ◽  
Carbene Complexes

KI/K 2 S 2 O 8 ‐Mediated C‐S/C‐N Bond Formation: One‐Pot Regioselective Synthesis of 5 H ‐Thiazolo[3,2‐a]pyrimidines

2019 ◽  
Vol 4 (21) ◽  
pp. 6583-6586 ◽  
Author(s):  
Zan Yang ◽  
Si Liu ◽  
An Li ◽  
Jiashu Liao ◽  
Lijun Li ◽  
...  
Keyword(s):  
Bond Formation ◽  
Regioselective Synthesis ◽  
One Pot

Microwave-accelerated Carbon-carbon and Carbon-heteroatom Bond Formation via Multi-component Reactions: A Brief Overview

2020 ◽  
Vol 7 (1) ◽  
pp. 23-39 ◽  
Author(s):  
Kantharaju Kamanna ◽  
Santosh Y. Khatavi
Keyword(s):  
Organic Synthesis ◽  
Bond Formation ◽  
Cycloaddition Reaction ◽  
Nanoparticle Synthesis ◽  
Single Step ◽  
Bioactive Molecules ◽  
One Pot ◽  
Bond Forming ◽  
Material Interest ◽  
Carbon Carbon Bond

Multi-Component Reactions (MCRs) have emerged as an excellent tool in organic chemistry for the synthesis of various bioactive molecules. Among these, one-pot MCRs are included, in which organic reactants react with domino in a single-step process. This has become an alternative platform for the organic chemists, because of their simple operation, less purification methods, no side product and faster reaction time. One of the important applications of the MCRs can be drawn in carbon- carbon (C-C) and carbon-heteroatom (C-X; X = N, O, S) bond formation, which is extensively used by the organic chemists to generate bioactive or useful material synthesis. Some of the key carbon- carbon bond forming reactions are Grignard, Wittig, Enolate alkylation, Aldol, Claisen condensation, Michael and more organic reactions. Alternatively, carbon-heteroatoms containing C-N, C-O, and C-S bond are also found more important and present in various heterocyclic compounds, which are of biological, pharmaceutical, and material interest. Thus, there is a clear scope for the discovery and development of cleaner reaction, faster reaction rate, atom economy and efficient one-pot synthesis for sustainable production of diverse and structurally complex organic molecules. Reactions that required hours to run completely in a conventional method can now be carried out within minutes. Thus, the application of microwave (MW) radiation in organic synthesis has become more promising considerable amount in resource-friendly and eco-friendly processes. The technique of microwaveassisted organic synthesis (MAOS) has successfully been employed in various material syntheses, such as transition metal-catalyzed cross-coupling, dipolar cycloaddition reaction, biomolecule synthesis, polymer formation, and the nanoparticle synthesis. The application of the microwave-technique in carbon-carbon and carbon-heteroatom bond formations via MCRs with major reported literature examples are discussed in this review.

scholarly journals Correction: One-pot three-component synthesis of 1-amidoalkyl naphthols and polyhydroquinolines using a deep eutectic solvent: a green method and mechanistic insight

2021 ◽  
Vol 45 (9) ◽  
pp. 4507-4507
Author(s):  
Vu Thanh Nguyen ◽  
Hai Truong Nguyen ◽  
Phuong Hoang Tran
Keyword(s):  
Deep Eutectic Solvent ◽  
Green Method ◽  
One Pot ◽  
Mechanistic Insight ◽  
Amidoalkyl Naphthols

Correction for ‘One-pot three-component synthesis of 1-amidoalkyl naphthols and polyhydroquinolines using a deep eutectic solvent: a green method and mechanistic insight’ by Vu Thanh Nguyen et al., New J. Chem., 2021, 45, 2053–2059, DOI: 10.1039/d0nj05687a.

ChemInform Abstract: A Three-Component Domino Reaction of 2-Tetralone, Hydroxylamine and Acetylene: A One-Pot, Highly Regioselective Synthesis of 4,5-Dihydrobenz[e]indoles.

ChemInform ◽  
2010 ◽  
Vol 41 (28) ◽  
pp. no-no
Author(s):  
Alexander M. Vasil'tsov ◽  
Andrei V. Ivanov ◽  
Al'bina I. Mikhaleva ◽  
Boris A. Trofimov
Keyword(s):  
Regioselective Synthesis ◽  
Domino Reaction ◽  
One Pot

Promiscuous lipase catalyzed a new P-C bond formation: Green and efficient protocol for one-pot synthesis of α-aminophosphonates

2017 ◽  
Vol 28 (6) ◽  
pp. e21408 ◽  
Author(s):  
Samia Guezane-Lakoud ◽  
Martial Toffano ◽  
Louisa Aribi-Zouioueche
Keyword(s):  
Bond Formation ◽  
One Pot ◽  
One Pot Synthesis
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