Stereoselective Synthesis of Multifunctionalized 1,2,4-Triazolidines by a Ruthenium Porphyrin-Catalyzed Three-Component Coupling Reaction

2006 ◽  
Vol 348 (16-17) ◽  
pp. 2391-2396 ◽  
Author(s):  
Ming-Zhong Wang ◽  
Hai-Wei Xu ◽  
Yungen Liu ◽  
Man-Kin Wong ◽  
Chi-Ming Che
Keyword(s):  
Stereoselective Synthesis ◽  
Coupling Reaction ◽  
Ruthenium Porphyrin ◽  
Three Component Coupling

scholarly journals N-Alkylation/aldol reaction of α-aldimino thioesters: a facile three-component coupling reaction

RSC Advances ◽  
2021 ◽  
Vol 11 (22) ◽  
pp. 13097-13104
Author(s):  
Makoto Shimizu ◽  
Asako Higashino ◽  
Isao Mizota ◽  
Yusong Zhu
Keyword(s):  
Aldol Reaction ◽  
Coupling Reaction ◽  
Three Component Coupling

Treatment of α-aldimino thioesters with dialkylzinc reagents in the presence of aldehydes or imines gives three-component coupling products in good yields with good to high anti-selectivities.

Pd-Catalyzed Coupling Reaction of Acetylenes, Iodotrimethylsilane, and Organozinc Reagents for the Stereoselective Synthesis of Vinylsilanes

1995 ◽  
Vol 60 (6) ◽  
pp. 1834-1840 ◽  
Author(s):  
Naoto Chatani ◽  
Nobuyoshi Amishiro ◽  
Takaya Morii ◽  
Toshiaki Yamashita ◽  
Shinji Murai
Keyword(s):  
Stereoselective Synthesis ◽  
Coupling Reaction ◽  
Organozinc Reagents

scholarly journals PEG-embedded KBr3: A recyclable catalyst for multicomponent coupling reaction for the efficient synthesis of functionalized piperidines

2011 ◽  
Vol 7 ◽  
pp. 1334-1341 ◽  
Author(s):  
Sanny Verma ◽  
Suman L Jain ◽  
Bir Sain
Keyword(s):  
Coupling Reaction ◽  
Recyclable Catalyst ◽  
Efficient Synthesis ◽  
Molecular Bromine ◽  
Keto Ester ◽  
One Step ◽  
High Yields ◽  
Multicomponent Coupling ◽  
Three Component Coupling

PEG-embedded potassium tribromide ([K+PEG]Br3 −) was found to be an efficient and recyclable catalyst for the synthesis of functionalized piperidines in high yields in a one step, three component coupling between aldehyde, amine and β-keto ester. At the end of the reaction the [K+PEG]Br3 − was readily regenerated from the reaction mixture by treating the residue containing [K+PEG]Br− with molecular bromine.

scholarly journals Preparation of Selanyl-Substituted Conjugated Enynes by Copper-Catalysed Coupling Reaction of (E)-γ-Selanyl Vinylzirconocene with Acetylenic Bromide

2003 ◽  
Vol 2003 (9) ◽  
pp. 584-585 ◽  
Author(s):  
Meihua Xie ◽  
Xian Huang
Keyword(s):  
Stereoselective Synthesis ◽  
Coupling Reaction ◽  
Conjugated Enynes

A stereoselective synthesis of conjugated enynes containing allyl selenide unit is reported. Selanyl-substituted conjugated enynes were obtained by the coupling reaction of ( E)-γ-selanyl vinylzirconocene with acetylenic bromide in the presence of CuCl.

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