Synthesis and relative stability of 3,5-diacyl-4,5-dihydro-1H-pyrazoles prepared by dipolar cycloaddition of enones and α-diazoketones

Journal of Organic Chemistry

Volumn 69, Issue 26, 2004, Pages 9085-9089

  Jung, Michael E ^a   Min, Sun Joon ^a   Houk, K N ^a   Ess, Daniel ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; ISOMERS; KETONES; MOLECULAR STRUCTURE; PROBABILITY DENSITY FUNCTION; SYNTHESIS (CHEMICAL);

ACETYL GROUPS; HETEROCYCLIC SYSTEMS; REACTION PROCESS; TRIKETONE;

ORGANIC COMPOUNDS;

3 ACETYL 2,6 HEPTANEDIONE; 3,5 DIACYL 4,5 DIHYDRO 1H PYRAZOLE DERIVATIVE; ACETIC ACID DERIVATIVE; ACETOPHENONE DERIVATIVE; ALPHA DIAZOACETOPHENONE; ALPHA DIAZOKETONE; ALPHA DIAZOMETHYL KETONE; AZIDE; BENZOYL DERIVATIVE; DIHYDROPYRAZOLE; FUNCTIONAL GROUP; HYDRAZONE DERIVATIVE; KETONE; METHANESULFONYL AZIDE; METHYLVINYL KETONE; PYRAZOLE DERIVATIVE; TRIFLUOROMETHYLTRIONE; UNCLASSIFIED DRUG;

ARTICLE; BOND LENGTH; CHEMICAL STRUCTURE; CONJUGATION; CYCLOADDITION; DENSITY FUNCTIONAL THEORY; ENERGY TRANSFER; FRAGMENTATION REACTION; FRAGMENTATION RECOMBINATION REACTION MECHANISM; MOLECULAR STABILITY; OXIDATION; QUANTUM CHEMISTRY; REACTION ANALYSIS; STEREOCHEMISTRY; STOICHIOMETRY; SYNTHESIS;

EID: 10844240709     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo048741w     Document Type: Article

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