Regio- and diastereoselectivity of the 1,3-dipolar cycloaddition of α-aryl nitrone with methacrolein. A theoretical investigation

RSC Advances ◽  
2015 ◽  
Vol 5 (28) ◽  
pp. 22126-22134 ◽  
Author(s):  
Wafaa Benchouk ◽  
Sidi Mohamed Mekelleche

The mechanism, regio- and diastereoselectivity of the 1,3-dipolar cycloaddition of N-iso-propyl,α-(4-trifluoromethyl)-phenyl nitrone with methacrolein yielding the isoxazolidine cycloadduct has been studied at the B3LYP/6-31G(d) level of theory.

2010 ◽  
Vol 51 (19) ◽  
pp. 2617-2621 ◽  
Author(s):  
Abdelmalek Khorief Nacereddine ◽  
Wassila Yahia ◽  
Samir Bouacha ◽  
Abdelhafid Djerourou

ChemPhysChem ◽  
2012 ◽  
Vol 13 (3) ◽  
pp. 741-750 ◽  
Author(s):  
Yanli Yuan ◽  
Peiyu Chen ◽  
Xingye Ren ◽  
Hongming Wang

RSC Advances ◽  
2021 ◽  
Vol 11 (52) ◽  
pp. 32792-32798
Author(s):  
Yang He ◽  
Dong-Hui Xu ◽  
Yan-Jun Zhang ◽  
Chun Zhang ◽  
Jian-Min Guo ◽  
...  

The microscopic mechanisms of light-induced tetrazole-quinone 1,3-dipolar cycloaddition are elucidated using high level MS-CASPT2 calculations.


Tetrahedron ◽  
2020 ◽  
Vol 76 (15) ◽  
pp. 131104 ◽  
Author(s):  
Mariia M. Efremova ◽  
Alexander P. Molchanov ◽  
Alexander S. Novikov ◽  
Galina L. Starova ◽  
Anna A. Muryleva ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document