Studies on chiral organosulfur compounds. VI. The use of a chiral diene bearing an optically active sulfinylmethyl group in the Lewis acid-catalyzed intramolecular asymmetric hetero Diels-Alder reaction

Chemical and Pharmaceutical Bulletin

Volumn 45, Issue 5, 1997, Pages 759-764

  Hiroi, Kunio ^a   Umemura, Masayuki ^a   Tomikawa, Yoko ^a   Kaneko, Masamitsu ^a   Kato, Fumiko ^a  

^a TOHOKU PHARMACEUTICAL UNIVERSITY   (Japan)

Author keywords

Asymmetric hetero Diels Alder reaction; Benzopyran; Chiral sulfinyl; Lewis acid

Indexed keywords

1 (4 TOLUENESULFINYL) 6,6,10 TRIMETHYL 3,9 UNDECADIEN 2 ONE; 4 BROMO 4A,5,6,7,8,8A HEXAHYDRO 1,1,3,6,6 PENTAMETHYL 1H 2 BENZOPYRAN; 4A,5,6,7,8,8A HEXAHYDRO 1,1,3,6,6 PENTAMETHYL 4 (4 TOLUENESULFINYL) 1H 2 BENZOPYRAN; 4A,5,6,7,8,8A HEXAHYDRO 1,1,6,6 TETRAMETHYL 2 (4 TOLUENESULFINYLMETHYL) 1H 2 BENZOPYRAN; BENZOPYRAN DERIVATIVE; CITRONELLAL; UNCLASSIFIED DRUG;

ARTICLE; CATALYST; CHEMICAL REACTION; CHIRALITY; OPTICAL ROTATION; STEREOCHEMISTRY; SYNTHESIS;

EID: 0030950583     PISSN: 00092363     EISSN: None     Source Type: Journal    
DOI: 10.1248/cpb.45.759     Document Type: Article

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