Theoretical study of the reaction mechanism and solvent effect on the regioselectivity of 1,3-dipolar cycloaddition reaction between azide and acetylene derivatives

2007 ◽  
Vol 18 (3) ◽  
pp. 203-207 ◽  
Author(s):  
Xi-Bo Li ◽  
Qin-Hua Song
2016 ◽  
Vol 90 (5) ◽  
pp. 1027-1033 ◽  
Author(s):  
Wenxing He ◽  
Hong Zhang ◽  
Nana Wang ◽  
Xiaojun Tan ◽  
Weihua Wang ◽  
...  

2016 ◽  
Vol 15 (3) ◽  
pp. 221-230 ◽  
Author(s):  
Wenxing He ◽  
Weihua Wang ◽  
Xiaojun Tan ◽  
Ping Li

2010 ◽  
Vol 12 (8) ◽  
pp. 1958 ◽  
Author(s):  
Cinzia Chiappe ◽  
Benedetta Mennucci ◽  
Christian Silvio Pomelli ◽  
Angelo Sanzone ◽  
Alberto Marra

SynOpen ◽  
2017 ◽  
Vol 01 (01) ◽  
pp. 0063-0067
Author(s):  
Sirisha Nallamala ◽  
Srikumar Mannem ◽  
Raghunathan Raghavachary

A variety of sugar-fused chromanono pyrrolidines/pyrrolizidines/thiolizidines have been synthesized by intermolecular 1,3-dipolar cycloaddition reaction of azomethine ylides (generated from glucose aldehyde and different secondary amino acids) with various 3-arylidene chroman-4-ones as dipolarophiles. The solvent effect on the 1,3-dipolar cycloaddition reaction is also studied.


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