Reaction of trifluororacemic acid methyl ester with 1,3-dienes
摘要:
The reaction of trifluororacemic acid with 1,3-dienes affords Diels-Alder reaction products in a high yield and with a high degree of specificity. Catalysis by SnCl4 changes the course of the reaction of the ester with isoprene, affording an ene reaction product.
SOLOSHONOK, V. A.;ROZHENKO, A. B.;BUTOVICH, I. A.;KUXAR, V. P., ZH. ORGAN. XIMII, 26,(1990) N0, S. 2051-2056
作者:SOLOSHONOK, V. A.、ROZHENKO, A. B.、BUTOVICH, I. A.、KUXAR, V. P.
DOI:——
日期:——
GOLUBEV, A. S.;GALAXOV, M. V.;KOLOMIETS, A. F.;FOKIN, A. V., IZV. AN CCCP. CEP. XIM.,(1991) N, S. 141-145
作者:GOLUBEV, A. S.、GALAXOV, M. V.、KOLOMIETS, A. F.、FOKIN, A. V.
DOI:——
日期:——
Soloshonok, V. A.; Rozhenko, A. B.; Butovich, I. A., Journal of Organic Chemistry USSR (English Translation), 1990, vol. 26, # 10, p. 1771 - 1775
作者:Soloshonok, V. A.、Rozhenko, A. B.、Butovich, I. A.、Kukhar', V. P.
DOI:——
日期:——
Reaction of trifluororacemic acid methyl ester with 1,3-dienes
作者:A. S. Golubev、M. V. Galakhov、A. F. Kolomiets、A. V. Fokin
DOI:10.1007/bf00959643
日期:1991.1
The reaction of trifluororacemic acid with 1,3-dienes affords Diels-Alder reaction products in a high yield and with a high degree of specificity. Catalysis by SnCl4 changes the course of the reaction of the ester with isoprene, affording an ene reaction product.