O. V. Gulyakevich, I. L. Rubinova, A. A. Govorova, I. P. Antonevich, L. P. Solovei, D. B. Rubinov, A. S. Lyakhov, Yu. S. Polyakov, A. L. Mikhal'chuk, “The annelation of 3,4-dihydroisoquinoline by 2-acetylcycloheptane-1,3-dione: the effect of 2-acylcycloalkane-1,3-dione ring size on the annelation of cyclic Schiff bases”, Mendeleev Commun., 2001, Volume 11, Issue 4,Pages <nobr>155

This article is cited in 4 papers

The annelation of 3,4-dihydroisoquinoline by 2-acetylcycloheptane-1,3-dione: the effect of 2-acylcycloalkane-1,3-dione ring size on the annelation of cyclic Schiff bases

O. V. Gulyakevich^a, I. L. Rubinova^a, A. A. Govorova^a, I. P. Antonevich^a, L. P. Solovei^a, D. B. Rubinov^a, A. S. Lyakhov^a, Yu. S. Polyakov^b, A. L. Mikhal'chuk^a

^a Institute of Bioorganic Chemistry, National Academy of Sciences of Belarus, Minsk, Belarus
^b Research Institute of Physical and Chemical Problems, Belarus State University, Minsk, Belarus

Abstract: New condensed 3,4-dihydroisoquinoline derivatives — 10,11-dimethoxy-1,2,3,4,5,7,8,12b,13,14-decahydrocyclohepta[5,6]pyrido-[2,1-a]isoquinoline-1,14-dione [or 2,3-dimethoxy-8-aza-D-dihomogona-1,3,5(10),13-tetraene-12,17b-dione] and 2,3-dimethoxy- 5,6,8,9,10,11,12,13,14,15,16,16a-dodecahydroazacycloundeca[2,1-a]isoquinoline-8,13,15-trione — have been obtained by the heteroannelation of 3,4-dihydroisoquinoline by 2-acetylcycloheptane-1,3-dione.

Language: English

DOI: 10.1070/MC2001v011n04ABEH001409