Thermodynamically controlled photocycloaddition of 5-fluoro-1,3-dimethyluracil to naphthalenes

Heterocycles

Volumn 58, Issue , 2002, Pages 595-600

  Ohkura, Kazue ^a   Sugaoi, Tatsuyuki ^a   Sakushima, Akiyo ^a   Nishijima, Ken ichi ^a,b   Kuge, Yuji ^b   Seki, Koh ichi ^a  

^a HEALTH SCIENCES UNIVERSITY OF HOKKAIDO   (Japan)

^b HOKKAIDO UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

1 ACETONAPHTHONE; 1 NAPHTHONITRILE; 5 FLUORO 1,3 DIMETHYLURACIL; ACETIC ACID DERIVATIVE; ACETONAPHTHONE; BENZENE DERIVATIVE; CARBON; CYANIDE; ETHENOBENZOQUINAZOLINE; ETHENOBENZOQUINAZOLINE 10 CARBONITRILE; NAPHTHALENE DERIVATIVE; NITRILE; QUINAZOLINE DERIVATIVE; UNCLASSIFIED DRUG; URACIL DERIVATIVE;

ARTICLE; CHEMICAL REACTION; CYCLOADDITION; ENVIRONMENTAL TEMPERATURE; ISOMER; KINETICS; PHOTOREACTIVITY; REACTION ANALYSIS; THERMODYNAMICS; ULTRAVIOLET RADIATION;

EID: 0037159793     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (9)

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8. 3
9. MO calculation was performed by the AM1 method with MOPAC on CAChe Work-system (Release 3.7; Cache Scientific, Inc.).