Diels-Alder cycloadditions of 2(1H)-quinolones having an electron-withdrawing group at the 3-position acting as dienophiles with dienes

Chemical and Pharmaceutical Bulletin

Volumn 49, Issue 7, 2001, Pages 893-899

  Fujita, R ^a   Watanabe, K ^a   Yoshisuji, T ^a   Kabuto, C ^a   Matsuzaki, H ^a   Hongo, H ^a  

^a TOHOKU PHARMACEUTICAL UNIVERSITY   (Japan)

Author keywords

3 Substituted 2(1H) quinolone; Chemoselectivity; Diels Alder cycloaddition; Electron withdrawing group; MO calculation; Regioselectivity

Indexed keywords

1,3 BUTADIENE DERIVATIVE; ALKADIENE; CARBOSTYRIL DERIVATIVE; PHENANTHRENE DERIVATIVE;

ARTICLE; ATMOSPHERIC PRESSURE; DRUG SYNTHESIS; ELECTRON TRANSPORT; REACTION ANALYSIS; STEREOCHEMISTRY;

CYCLIZATION; ELECTRONS; INDICATORS AND REAGENTS; MAGNETIC RESONANCE SPECTROSCOPY; MODELS, MOLECULAR; MOLECULAR CONFORMATION; OXIDATION-REDUCTION; QUINOLONES; STEREOISOMERISM;

EID: 0034945748     PISSN: 00092363     EISSN: None     Source Type: Journal    
DOI: 10.1248/cpb.49.893     Document Type: Article

References (27)