Nitrile oxide [3+ 2] cycloaddition: application to the synthesis of 6-substituted 3 (2H)-pyridazinones and 6-substituted 4, 5-Dihydro-4-hydroxy-3 (2H)-pyridazinones
…, B Cacciari, C Caldari, S Manfredini, G Spalluto
Index: Baraldi; Bigoni; Cacciari; Caldari; Manfredini; Spalluto Synthesis, 1994 , # 11 p. 1158 - 1162
Full Text: HTML
Citation Number: 28
Abstract
An eflicient method for the preparation of 6-substituted 3 (2H)-pyridazinones and 6- substituted 4, 5-dihydro-4-hydroxy-3 (2H)-py-ridazinones starting from 3, 5-disubstituted 4, 5- dihydroisoxazoles is described. N—O bond cleavage of the isoxazoline ring promoted by molybdenum hexacarbonyl or by catalytic hydrogenation afiordcd the oz-hydroxy y-keto esters 4a—f which were converted into 6-substituted 4, 5-dihydro-4-hydroxy-3 (2H)- ...
Related Articles:
[Xing, Xuechao; Chang, Ling-Chu; Kong, Qiongman; Colton, Craig K.; Lai, Liching; Glicksman, Marcie A.; Lin, Chien-Liang Glenn; Cuny, Gregory D. Bioorganic and Medicinal Chemistry Letters, 2011 , vol. 21, # 19 p. 5774 - 5777]
[Xing, Xuechao; Chang, Ling-Chu; Kong, Qiongman; Colton, Craig K.; Lai, Liching; Glicksman, Marcie A.; Lin, Chien-Liang Glenn; Cuny, Gregory D. Bioorganic and Medicinal Chemistry Letters, 2011 , vol. 21, # 19 p. 5774 - 5777]