Nitro olefins and organoaluminum compounds: a powerful synthetic tool in organic chemistry
A Pecunioso, R Menicagli
Index: Pecunioso, Angelo; Menicagli, Rita Journal of Organic Chemistry, 1989 , vol. 54, # 10 p. 2391 - 2396
Full Text: HTML
Citation Number: 41
Abstract
[R m] M species react with a-nitro olefins showing an unusual aptitude for a preferential transfer of saturated alkyl groups;[R2AlR'2] M (R'= phenyl, benzyl, allyl) species, on the other hand, are able to transfer unsaturated groups with high chemoselectivity. In particular, dialkyldiallylalanates react with a-nitro olefins to give either &nitro olefins or the corresponding y, &unsaturated ketones in very good yields. This reaction, synthetically ...
Related Articles:
[Nagano; Sugihara; Harada; Fukuchi; Yamada; Izawa; Shiota Bulletin of the Chemical Society of Japan, 1990 , vol. 63, # 12 p. 3560 - 3565]
[Ballini Synthesis, 1993 , # 7 p. 687 - 688]
[Matsuda, Isamu; Murata, Shizuaki; Izumi, Yusuke Journal of Organic Chemistry, 1980 , vol. 45, # 2 p. 237 - 240]
[Betancourt de Perez, Rosa M.; Fuentes, Lelia M.; Larson, Gerald L.; Barnes, Charles L.; Heeg, Mary Jane Journal of Organic Chemistry, 1986 , vol. 51, # 11 p. 2039 - 2043]
[Ballini Synthesis, 1993 , # 7 p. 687 - 688]