Ontology type: schema:ScholarlyArticle
2005-06
AUTHORSA. B. Zaitsev, E. Yu. Schmidt, A. M. Mikhaleva, A. V. Afonin, I. A. Ushakov
ABSTRACTDioximes of 1,3-diketones enter into the Trofimov reaction forming pyrroles containing an acyl or an O-vinyloxime substituent in position 3 of the pyrrole. In the case of sterically hindered dioximes the main reaction products are isoxazoles.
PAGES722-729
http://scigraph.springernature.com/pub.10.1007/s10593-005-0212-6
DOIhttp://dx.doi.org/10.1007/s10593-005-0212-6
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