A rational protocol for the synthesis of 1-(2-pyridyl)isoquinolines / Kopchuk Dmitry S.,Kovalev Igor S.,Khasanov Albert F.,Zyryanov Grigory V.,Slepukhin Pavel A.,Rusinov Vladimir L.,Chupakhin Oleg N. // MENDELEEV COMMUNICATIONS. - 2013. - V. 23, l. 3. - P. 142-144.

ISSN/EISSN:
0959-9436 / 1364-551X
Type:
Article
Abstract:
Aza-Diels-Alder reaction between 3-(2-pyridyl)-1,2,4-triazines and 1-morpholinocyclohexene followed by aromatization of the cyclohexene moiety affords 1-(2-pyridyl)isoquinolines. Crystal structures of two tetrahydroisoquinolines were confirmed by X-ray diffraction analysis.
Author keywords:
DIELS-ALDER REACTION; INVERSE ELECTRON DEMAND; ISOQUINOLINE ALKALOIDS; SUBSTITUTED PYRIDINES; ASYMMETRIC-SYNTHESIS; IRIDIUM COMPLEXES; 1,2,4-TRIAZINES; LIGANDS; 2,2'-BIPYRIDINE; CYCLOADDITION
DOI:
10.1016/j.mencom.2013.05.007
Web of Science ID:
ISI:000321540500007
Соавторы в МНС:
Другие поля
Поле Значение
Month MAY-JUN
Publisher ELSEVIER SCIENCE BV
Address PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS
Language English
EISSN 1364-551X
Keywords-Plus DIELS-ALDER REACTION; INVERSE ELECTRON DEMAND; ISOQUINOLINE ALKALOIDS; SUBSTITUTED PYRIDINES; ASYMMETRIC-SYNTHESIS; IRIDIUM COMPLEXES; 1,2,4-TRIAZINES; LIGANDS; 2,2'-BIPYRIDINE; CYCLOADDITION
Research-Areas Chemistry
Web-of-Science-Categories Chemistry, Multidisciplinary
Author-Email dkopchuk@mail.ru
Funding-Acknowledgement Russian Ministry of Education and Science {[}14.740.11.1020, 14.A18.21.0817]; Russian Foundation for Basic Research {[}12-03-31726]; Council for grants of the President of the Russian Federation {[}MK-1511.2013.3]
Funding-Text The work was supported by the Russian Ministry of Education and Science (state contract nos. 14.740.11.1020 and 14.A18.21.0817), the Russian Foundation for Basic Research (grant no. 12-03-31726) and the Council for grants of the President of the Russian Federation (grant no. MK-1511.2013.3).
Number-of-Cited-References 58
Usage-Count-Last-180-days 2
Usage-Count-Since-2013 5
Journal-ISO Mendeleev Commun.
Doc-Delivery-Number 179SB