ChemInform Abstract: One-Pot Synthesis of 1,4-Dihydropyridines via a Phenylboronic Acid Catalyzed Hantzsch Three-Component Reaction.

ChemInform ◽  
2008 ◽  
Vol 39 (27) ◽  
Author(s):  
Abdelmadjid Debache ◽  
Raouf Boulcina ◽  
Ali Belfaitah ◽  
Salah Rhouati ◽  
Bertrand Carboni
Keyword(s):  
Phenylboronic Acid ◽  
One Pot ◽  
One Pot Synthesis ◽  
Three Component Reaction ◽  
Acid Catalyzed

One-Pot Synthesis of 1,4-Dihydropyridines via a Phenylboronic Acid Catalyzed Hantzsch Three-Component Reaction

Synlett ◽  
2008 ◽  
Vol 2008 (04) ◽  
pp. 509-512 ◽  
Author(s):  
Abdelmadjid Debache ◽  
Raouf Boulcina ◽  
Ali Belfaitah ◽  
Salah Rhouati ◽  
Bertrand Carboni
Keyword(s):  
Phenylboronic Acid ◽  
One Pot ◽  
One Pot Synthesis ◽  
Three Component Reaction ◽  
Acid Catalyzed

Phenylboronic acid catalyzed-cyanide promoted, one-pot synthesis of 2-(2-hydroxyphenyl)benzoxazole derivatives

2011 ◽  
Vol 52 (33) ◽  
pp. 4308-4312 ◽  
Author(s):  
Heraclio López-Ruiz ◽  
Horacio Briseño-Ortega ◽  
Susana Rojas-Lima ◽  
Rosa Santillan ◽  
Norberto Farfán
Keyword(s):  
Phenylboronic Acid ◽  
One Pot ◽  
One Pot Synthesis ◽  
Acid Catalyzed

One-Pot Synthesis of N -Alkyl Benzotriazoles via a Brønsted Acid-Catalyzed Three-Component Reaction

2017 ◽  
Vol 360 (2) ◽  
pp. 374-378 ◽  
Author(s):  
Xiangdong Wang ◽  
Chunqi Jia ◽  
Yadong Feng ◽  
Lianhui Wang ◽  
Xiuling Cui
Keyword(s):  
Bronsted Acid ◽  
Brønsted Acid ◽  
One Pot ◽  
One Pot Synthesis ◽  
Brönsted Acid ◽  
Three Component Reaction ◽  
Acid Catalyzed

ChemInform Abstract: Phenylboronic Acid Catalyzed-Cyanide-Promoted, One-Pot Synthesis of 2-(2-Hydroxyphenyl)benzoxazole Derivatives.

ChemInform ◽  
2011 ◽  
Vol 42 (46) ◽  
pp. no-no
Author(s):  
Heraclio Lopez-Ruiz ◽  
Horacio Briseno-Ortega ◽  
Susana Rojas-Lima ◽  
Rosa Santillan ◽  
Norberto Farfan
Keyword(s):  
Phenylboronic Acid ◽  
One Pot ◽  
One Pot Synthesis ◽  
Acid Catalyzed

Novel One-pot Synthesis of Pyranocarbazole Derivatives via an Isocyanide-based Three-component Reaction

2020 ◽  
Vol 17 ◽  
Author(s):  
Visarapu Malathi ◽  
Pedavenkatagari Narayana Reddy ◽  
Pannala Padmaja
Keyword(s):  
Efficient Method ◽  
Atom Economy ◽  
Reaction Conditions ◽  
One Pot ◽  
Catalyst Free ◽  
One Pot Synthesis ◽  
Three Component Reaction ◽  
High Yields

Abstract:: An efficient method has been developed for the synthesis of new pyrano[3,2-c] and pyrano[3,2-a]carbazole de-rivatives via a three component reaction of 4-hydroxycarbazole or 2-hydroxycarbazole, isocyanides, and dialkylacetylenedi-carboxylates. Noteworthy features of this protocol include mild reaction conditions, catalyst-free, high atom-economy and high yields.

ChemInform Abstract: Polymer-Supported Sulfonic Acid Catalyzed Three-Component One-Pot Synthesis of α-Amidoalkyl-β-naphthols.

ChemInform ◽  
2009 ◽  
Vol 40 (11) ◽  
Author(s):  
Li-Tao An ◽  
Xiao-Hua Lu ◽  
Fei-Qing Ding ◽  
Wen-Qing Jiang ◽  
Jian-Ping Zou
Keyword(s):  
Sulfonic Acid ◽  
One Pot ◽  
One Pot Synthesis ◽  
Acid Catalyzed ◽  
Polymer Supported

A heavy metal- and oxidant-free, one-pot synthesis of pyridines and fused pyridines based on a Lewis acid-catalyzed multicomponent reaction

2014 ◽  
Vol 50 (82) ◽  
pp. 12270-12272 ◽  
Author(s):  
V. P. Alex Raja ◽  
Giammarco Tenti ◽  
Subbu Perumal ◽  
J. Carlos Menéndez
Keyword(s):  
Heavy Metal ◽  
Lewis Acid ◽  
Multicomponent Reaction ◽  
One Pot ◽  
One Pot Synthesis ◽  
Acid Catalyzed

Pyridines and fused pyridines are accessible by a combination of a Lewis acid-catalyzed multicomponent reaction and aromatization involving loss of a 2-furylmethyl chain.

Isocyanide-based three component reaction for synthesis of highly cyano substituted furan derivatives

RSC Advances ◽  
2016 ◽  
Vol 6 (32) ◽  
pp. 26783-26790 ◽  
Author(s):  
Hamid Reza Safaei ◽  
Farbod Dehbozorgi
Keyword(s):  
Solvent Free ◽  
One Pot ◽  
Furan Derivatives ◽  
Catalyst Free ◽  
One Pot Synthesis ◽  
Three Component Reaction

A rapid and efficient solvent-free one-pot synthesis of novel alkyl amino aryl furan tricarbonitrile derivatives is described under catalyst-free conditions.

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