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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. Gulyakevicha,
I. L. Rubinovaa,
A. A. Govorovaa,
I. P. Antonevicha,
L. P. Soloveia,
D. B. Rubinova,
A. S. Lyakhova,
Yu. S. Polyakovb,
A. L. Mikhal'chuka 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
Аннотация:
New condensed 3,4-dihydroisoquinoline derivatives — 10,11-dimethoxy-1,2,3,4,5,7,8,12
b,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-12,17
b-dione] and 2,3-dimethoxy- 5,6,8,9,10,11,12,13,14,15,16,16
a-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.
Язык публикации: английский
DOI:
10.1070/MC2001v011n04ABEH001409