An Efficient Synthesis of New Dispiropyrrolidine DerivativesviaThree-Component 1,3-Dipolar Cycloaddition Reaction

2013 ◽  
Vol 50 (S1) ◽  
pp. E121-E125 ◽  
Author(s):  
Yu Hu ◽  
Da-Qing Shi
Keyword(s):  
Cycloaddition Reaction ◽  
Dipolar Cycloaddition ◽  
Efficient Synthesis

scholarly journals Efficient synthesis of some new antiproliferative N-fused indoles and isoquinolines via 1,3-dipolar cycloaddition reaction in an ionic liquid

2015 ◽  
Vol 39 (4) ◽  
pp. 2657-2668 ◽  
Author(s):  
Tushar R. Sutariya ◽  
Balvantsingh M. Labana ◽  
Narsidas J. Parmar ◽  
Rajni Kant ◽  
Vivek K. Gupta ◽  
...  
Keyword(s):  
Ionic Liquid ◽  
Cycloaddition Reaction ◽  
Reaction Medium ◽  
Environmentally Friendly ◽  
Dipolar Cycloaddition ◽  
Efficient Synthesis ◽  
Triethylammonium Acetate

Triethylammonium acetate (TEAA) as a new, recyclable and environmentally friendly reaction medium for the intramolecular[3+2] cycloaddition reaction.

Highly enantioselective catalytic 1,3-dipolar cycloadditions of α-alkyl diazoacetates: efficient synthesis of functionalized 2-pyrazolines

2015 ◽  
Vol 13 (9) ◽  
pp. 2745-2749 ◽  
Author(s):  
Sung Il Lee ◽  
Ka Eun Kim ◽  
Geum-Sook Hwang ◽  
Do Hyun Ryu
Keyword(s):  
Cycloaddition Reaction ◽  
Dipolar Cycloaddition ◽  
Efficient Synthesis ◽  
Dipolar Cycloadditions

Chiral oxazaborolidinium ion catalyzed 1,3-dipolar cycloaddition reaction of α-substituted diazoacetates gives functionalized 2-pyrazolines in high to excellent enantiomeric ratios.

ChemInform Abstract: Efficient Synthesis of Some New Antiproliferative N-Fused Indoles and Isoquinolines via 1,3-Dipolar Cycloaddition Reaction in an Ionic Liquid.

ChemInform ◽  
2015 ◽  
Vol 46 (33) ◽  
pp. no-no
Author(s):  
Tushar R. Sutariya ◽  
Balvantsingh M. Labana ◽  
Narsidas J. Parmar ◽  
Rajni Kant ◽  
Vivek K. Gupta ◽  
...  
Keyword(s):  
Ionic Liquid ◽  
Cycloaddition Reaction ◽  
Dipolar Cycloaddition ◽  
Efficient Synthesis

A facile and efficient synthesis of polycyclic spiropyrrolidine oxindoles bearing mesityl oxide unit via a three-component 1,3-dipolar cycloaddition reaction

Tetrahedron ◽  
2015 ◽  
Vol 71 (42) ◽  
pp. 8131-8139 ◽  
Author(s):  
Hui-Juan Wang ◽  
Bo-Wen Pan ◽  
Wen-Hui Zhang ◽  
Chao Yang ◽  
Xiong-Li Liu ◽  
...  
Keyword(s):  
Cycloaddition Reaction ◽  
Mesityl Oxide ◽  
Dipolar Cycloaddition ◽  
Efficient Synthesis

scholarly journals Efficient Synthesis of Dispiropyrrolidines Linked to Sugars

2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
Sirisha Nallamala ◽  
Raghavachary Raghunathan
Keyword(s):  
Cycloaddition Reaction ◽  
Azomethine Ylides ◽  
Dipolar Cycloaddition ◽  
The Novel ◽  
Efficient Synthesis

An expedient method for the synthesis of glyco-dispiropyrrolidines is reported through 1,3-dipolar cycloaddition reaction (1,3 DC reaction). The novel glycosyl dipolarophiles derived from D-glucose underwent neat [3+2] cycloaddition reaction with the azomethine ylides generated from 1,2-diketones and sarcosine to give the corresponding glycosidic heterocycles in good yields.

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