Consecutive nucleophilic substitution and aza Diels-Alder reaction - an efficient strategy to functionalized 2,2 `-bipyridines / Kozhevnikov DN,Kozhevnikov VN,Prokhorov AM,Ustinova MM,Rusinov VL,Chupakhin ON,Aleksandrov GG,Konig B // TETRAHEDRON LETTERS. - 2006. - V. 47, l. 6. - P. 869-872.

ISSN/EISSN:

0040-4039 / нет данных

Type:

Article

Abstract:

An efficient strategy for the synthesis of functionalized 2,2'-bipyridines is reported. The strategy is based on readily available 3-pyridyl-1,2,4-triazine 4-oxides and uses a reaction sequence of nucleophilic substitution of hydrogen and aza Diels-Alder reaction. (c) 2005 Elsevier Ltd. All rights reserved.

Author keywords:

COMPLEXES; PYRIDINE; LIGANDS; PHOTOPHYSICS; TERPYRIDINE; BIPYRIDINE; CHEMISTRY; CRYSTAL; FACILE

DOI:

10.1016/j.tetlet.2005.12.006

Web of Science ID:

ISI:000234953300004

Соавторы в МНС:

Другие поля

Поле	Значение
Month	FEB 6
Publisher	PERGAMON-ELSEVIER SCIENCE LTD
Address	THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND
Language	English
Keywords-Plus	COMPLEXES; PYRIDINE; LIGANDS; PHOTOPHYSICS; TERPYRIDINE; BIPYRIDINE; CHEMISTRY; CRYSTAL; FACILE
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Organic
Author-Email	dnk@htf.ustu.ru
ResearcherID-Numbers	Koenig, Burkhard/A-1362-2009 Prokhorov, Anton/B-9789-2011 Kozhevnikov, Valery/B-1178-2010
ORCID-Numbers	Koenig, Burkhard/0000-0002-6131-4850 Kozhevnikov, Valery/0000-0001-7032-8886
Number-of-Cited-References	23
Usage-Count-Since-2013	4
Journal-ISO	Tetrahedron Lett.
Doc-Delivery-Number	007FF