The role of the trifluoromethyl group in reactivity and selectivity in polar cycloaddition reactions. A DFT study

Tetrahedron

Volumn 68, Issue 40, 2012, Pages 8457-8462

  Sobhi, Chafia ^a   Nacereddine, Abdelmalek Khorief ^a   Djerourou, Abdelhafid ^a   Aurell, M Jose ^b   Domingo, Luis R ^b  

^a BADJI MOKHTAR UNIVERSITY   (Algeria)

^b UNIVERSITY OF VALENCIA   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

3,3,3 TRIFLUORO 1 NITROPROPENE; 3,3,3 TRIFLUORO 2 NITROPROPENE; ETHYLENE DERIVATIVE; NITRONE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL ANALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE; CONJUGATION; CYCLOADDITION; DENSITY FUNCTIONAL THEORY; DIASTEREOISOMER; ELECTROPHILICITY; NUCLEOPHILICITY; PRIORITY JOURNAL; STEREOCHEMISTRY; STRUCTURE ANALYSIS; SUBSTITUTION REACTION; THERMODYNAMICS;

TRIFLUORO;

EID: 84865394355     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2012.07.085     Document Type: Article

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