Electrophilically activated nitroalkanes in the synthesis of 6,7-dihydro-1H-cyclopenta[g]perimidines
摘要:
A highly efficient synthetic route to 6,7-dihydro-1H-cyclopenta[gh]perimidines has been proposed on the basis of a novel reaction of nitroalkanes with 4,5-diaminoacenaphthene in the presence of polyphosphoric acid. The reaction involves phosphorylation of the aci-nitro compound, followed by intramolecular cyclization.
Electrophilically activated nitroalkanes in the synthesis of 6,7-dihydro-1H-cyclopenta[g]perimidines
作者:A. V. Aksenov、N. A. Aksenov、D. S. Ovcharov、S. V. Shcherbakov、A. N. Smirnova、I. V. Aksenova、V. I. Goncharov、M. A. Rubin
DOI:10.1134/s107042801707020x
日期:2017.7
A highly efficient synthetic route to 6,7-dihydro-1H-cyclopenta[gh]perimidines has been proposed on the basis of a novel reaction of nitroalkanes with 4,5-diaminoacenaphthene in the presence of polyphosphoric acid. The reaction involves phosphorylation of the aci-nitro compound, followed by intramolecular cyclization.
POZHARSKIJ A. F.; KOROLEVA V. N.; GREKOVA I. F.; KASHPAROV I. S., XIMIYA GETEROTSIKL. SOEDIN. <KGSS-AQ>, 1975, HO 4, 557-560
作者:POZHARSKIJ A. F.、 KOROLEVA V. N.、 GREKOVA I. F.、 KASHPAROV I. S.