Detail of "4437-51-8"

Reference

1,2-Dioximes in the Trofimov reaction

All Rights Reserved. 1,2-Dioximes in the Trofimov reaction. Zaitsev, A. B.; Schmidt, E. Yu.; Vasil'tsov, A. M.; Mikhaleva, A. I.There are some reagents like 4437-51-8 is used in this study.; Petrova, O. V.; Afonin, A. V.; Zorina, N. V. (A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk, Russia). Chemistry of Heterocyclic Compounds (New York, NY, United States), 42(1), 34-41 (English) 2006 Springer. CODEN: CHCCAL. ISSN: 0009-3122. There are some commonly used reagents like 4437-51-8 in this article. DOCUMENT TYPE: Journal CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) Section cross-reference(s): 27 3,3'-Dimethyl-1,1'-divinyl-2,2'-bipyrrole (I) was obtained during the reaction of 3,4-hexanedione dioxime with acetylene under pressure in the potassium hydroxide-DMSO system. In the case of 1,2-cyclohexanedione dioxime, fused pyrroles II, III, and IV were isolated. a-Benzil and a-furil dioximes gave 1,2,5-oxadiazoles (V; R = Ph, 2-furanyl, resp.), in addn. to their mono- and divinyl derivs. ..

1,2-Dioximes in the Trofimov reaction

All Rights Reserved. 1,2-Dioximes in the Trofimov reaction. Zaitsev, A. B.; Schmidt, E. Yu.; Vasil'tsov, A. M.; Mikhaleva, A. I.There are some reagents like 4437-51-8 is used in this study.; Petrova, O. V.; Afonin, A. V.; Zorina, N. V. (A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, Irkutsk, Russia). Chemistry of Heterocyclic Compounds (New York, NY, United States), 42(1), 34-41 (English) 2006 Springer. CODEN: CHCCAL. ISSN: 0009-3122. There are some commonly used reagents like 4437-51-8 in this article. DOCUMENT TYPE: Journal CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) Section cross-reference(s): 27 3,3'-Dimethyl-1,1'-divinyl-2,2'-bipyrrole (I) was obtained during the reaction of 3,4-hexanedione dioxime with acetylene under pressure in the potassium hydroxide-DMSO system. In the case of 1,2-cyclohexanedione dioxime, fused pyrroles II, III, and IV were isolated. a-Benzil and a-furil dioximes gave 1,2,5-oxadiazoles (V; R = Ph, 2-furanyl, resp.), in addn. to their mono- and divinyl derivs. ..