Results 181 to 190 of about 24,842 (217)
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Organic Letters, 2016
A highly enantioselective 1,3-dipolar cycloaddition of imino esters with methyleneindolinones has been realized by using readily available thiourea-quaternary ammonium salts as phase-transfer catalysts, enabling efficient construction of a range of ...
Jiaxing Zhang+5 more
semanticscholar +1 more source
A highly enantioselective 1,3-dipolar cycloaddition of imino esters with methyleneindolinones has been realized by using readily available thiourea-quaternary ammonium salts as phase-transfer catalysts, enabling efficient construction of a range of ...
Jiaxing Zhang+5 more
semanticscholar +1 more source
Chemical Communications, 2015
A new strategy for the construction of optically active 5'-CF3 spiro[pyrrolidin-3,2'-oxindole] was described. A series of unprecedented 1,3-dipoles were obtained by condensation of CF3CH2NH2 with isatins.
M. Ma+10 more
semanticscholar +1 more source
A new strategy for the construction of optically active 5'-CF3 spiro[pyrrolidin-3,2'-oxindole] was described. A series of unprecedented 1,3-dipoles were obtained by condensation of CF3CH2NH2 with isatins.
M. Ma+10 more
semanticscholar +1 more source
1,3-Dipolar Cycloadditions in Aqueous Media
HETEROCYCLES, 2006AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
openaire +4 more sources
Angewandte Chemie, 2016
The use of alkenyl arenes as dipolarophiles in the catalytic asymmetric 1,3-dipolar cycloaddition of azomethine ylides is reported. Under appropriate reaction conditions with a CuI or AgI catalyst either the exo or the endo adduct was obtained with high ...
Ana Pascual-Escudero+4 more
semanticscholar +1 more source
The use of alkenyl arenes as dipolarophiles in the catalytic asymmetric 1,3-dipolar cycloaddition of azomethine ylides is reported. Under appropriate reaction conditions with a CuI or AgI catalyst either the exo or the endo adduct was obtained with high ...
Ana Pascual-Escudero+4 more
semanticscholar +1 more source
Angewandte Chemie, 2017
In the long history of corannulene chemistry, the 1,3-dipolar cycloaddition to corannulene is unprecedented. Reported herein is the 1,3-dipolar cycloaddition of a polycyclic aromatic azomethine ylide to corannulene, a reaction which occurs exclusively at
Yuki Tokimaru, S. Ito, K. Nozaki
semanticscholar +1 more source
In the long history of corannulene chemistry, the 1,3-dipolar cycloaddition to corannulene is unprecedented. Reported herein is the 1,3-dipolar cycloaddition of a polycyclic aromatic azomethine ylide to corannulene, a reaction which occurs exclusively at
Yuki Tokimaru, S. Ito, K. Nozaki
semanticscholar +1 more source
, 2017
A series of recoverable and reusable N-heterocyclic carbene silver complexes supported on polyacrylonitrile fiber were prepared and characterized. Their catalytic performances in three-component coupling reactions of aldehydes, amines, and alkynes (A3 ...
Jian Cao+4 more
semanticscholar +1 more source
A series of recoverable and reusable N-heterocyclic carbene silver complexes supported on polyacrylonitrile fiber were prepared and characterized. Their catalytic performances in three-component coupling reactions of aldehydes, amines, and alkynes (A3 ...
Jian Cao+4 more
semanticscholar +1 more source
Angewandte Chemie, 2017
2-Pyridylsulfone- and fluoroalkylated group-activated olefins underwent highly efficient diastereo- and enantioselective 1,3-dipolar cycloadditions across various aromatic and aliphatic nitrones in the presence of a chiral NiII /bis(oxazoline) catalyst ...
Xing Yang+6 more
semanticscholar +1 more source
2-Pyridylsulfone- and fluoroalkylated group-activated olefins underwent highly efficient diastereo- and enantioselective 1,3-dipolar cycloadditions across various aromatic and aliphatic nitrones in the presence of a chiral NiII /bis(oxazoline) catalyst ...
Xing Yang+6 more
semanticscholar +1 more source
ChemInform Abstract: Enantioselective Copper‐Catalyzed 1,3‐Dipolar Cycloadditions
ChemInform, 2008AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Levi M. Stanley, Mukund P. Sibi
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What Controls the Reactivity of 1,3‐Dipolar Cycloadditions?
Angewandte Chemie International Edition, 2009AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Bernd Engels, Manfred Christl
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Organic Letters, 2014
A p-TsOH-mediated 1,3-dipolar cycloaddition of nitroolefins and sodium azide for the synthesis of 4-aryl-NH-1,2,3-triazoles has been developed. p-TsOH was discovered as a vital additive in this type of 1,3-dipolar cycloaddition.
Xu Quan+3 more
semanticscholar +1 more source
A p-TsOH-mediated 1,3-dipolar cycloaddition of nitroolefins and sodium azide for the synthesis of 4-aryl-NH-1,2,3-triazoles has been developed. p-TsOH was discovered as a vital additive in this type of 1,3-dipolar cycloaddition.
Xu Quan+3 more
semanticscholar +1 more source