Theoretical analysis and experimental study of the spatial structure and isomerism of acetone azine and its cyclization to 3,5,5-trimethyl-4,5-dihydro- 1H-pyrazole

Journal of Structural Chemistry

Volumn 45, Issue 5, 2004, Pages 748-755

  Kobychev, V B ^a   Vitkovskaya, N M ^a   Pavlova, N V ^a   Schmidt, E Yu ^b   Trofimov, B A ^b  

^a IRKUTSK STATE UNIVERSITY   (Russian Federation)

^b A E FAVORSKY IRKUTSK INSTITUTE OF CHEMISTRY   (Russian Federation)

Author keywords

3,5,5 Trimethyl 4,5 dihydro 1H pyrazole; ab initio calculations; Acetone azine; Cyclization; Internal rotation; Isomerization

Indexed keywords

1,3 BUTADIENE; ACETONE; ACYCLIC HYDROCARBON SUBSTITUENT; CARBON; HYDRAZINE DERIVATIVE; HYDRAZONE DERIVATIVE; NITROGEN; PYRAZOLE DERIVATIVE; VINYL DERIVATIVE;

ARTICLE; CHEMICAL BOND; CHEMICAL INTERACTION; CHEMICAL STRUCTURE; CYCLIZATION; ELECTRON; EXPERIMENTAL TEST; ISOMER; ISOMERISM; STEREOSPECIFICITY; THEORETICAL STUDY; THERMODYNAMICS; THERMOSTABILITY;

EID: 21644479007     PISSN: 00224766     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10947-005-0054-1     Document Type: Article

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