Cycloaddition routes to azaanthraquinone derivatives. 2. Use of azadienes
…, EB Walsh, D Bhattacharjee
Index: Potts, Kevin T.; Walsh, Eileen B.; Bhattacharjee Debkumar Journal of Organic Chemistry, 1987 , vol. 52, # 11 p. 2285 - 2292
Full Text: HTML
Citation Number: 60
Abstract
Azanaphthoquinones and l-(dimethylamino)-3-methyl-l-azabuta-1, 3-diene (methacrolein NJV-dimethylhydrazone) underwent extremely facile cycloaddition to aza-and polyazaanthraquinones after elimination of dimethylamine from the initial 1: l cycloadduct and ita subsequent oxidation. Introduction of a basic side chain into the &position of the azaanthraquinone occurred readily with primary amines and the 8-(tosyloxy) derivative, ...
Related Articles:
[Lee, Heesoon; Lee, Seung-Il; Yang, Sung-Il Bioorganic and Medicinal Chemistry Letters, 1998 , vol. 8, # 21 p. 2991 - 2994]
[Gesto, C.; Cuesta, E. de la; Avendano, C. Tetrahedron, 1989 , vol. 45, # 14 p. 4477 - 4484]