Electroorganic chemistry. Part 58. New synthesis of cyclopropanes from 1, 3-dicarbonyl compounds utilizing electroreduction of 1, 3-dimethanesulfonates
…, Y Matsumura, K Tsubata, Y Sugihara
Index: Shono, Tatsuyo; Matsumura, Yoshihiro; Tsubata, Kenji; Sugihara, Yoshihiro Journal of Organic Chemistry, 1982 , vol. 47, # 16 p. 3090 - 3094
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Citation Number: 19
Abstract
Discussion Two methanesulfonate groups seem essential to carry out this l, &elimination satisfactorily, since other leaving groups such as OH and OTHP brought about the formation of a mixture of products. Thus, the products from 18b were 37 and 38 in 70% and 23% yields, respectively, and 18c gave cyclopropane 19 (45%) and 39 (47%)(eq 10 and 11).
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