Nucleophilic aromatic substitution of hydrogen and related reactions / Charushin Valery N.,Chupakhin Oleg N. // MENDELEEV COMMUNICATIONS. - 2007. - V. 17, l. 5. - P. 249-254.

ISSN/EISSN:

0959-9436 / 1364-551X

Type:

Article

Abstract:

The classical concept of nucleophilic aromatic substitution (SNAripso) has been complemented with a new synthetic methodology (S-N(H)), enabling one to build new carbon-carbon C(sp(2))-C(sp(3)), C(sp(2))-C(sp(2)) and C(sp(2))-C(sp(2)) or carbon-heteroatom C(sp(2))-X (X is O, N, P, S, halogen) bonds through nucleophilic displacement of hydrogen in an aromatic ring.

Author keywords:

N-ALKYLAZINIUM CATIONS; ONE-STEP ROUTE; CONDENSED 1,2,4-TRIAZINES; TANDEM A(N)-A(N); LIQUID-AMMONIA; NITRO-GROUP; DERIVATIVES; CHEMISTRY; AZINES; SALTS

DOI:

10.1016/j.mencom.2007.09.001

Web of Science ID:

ISI:000250942700001

Соавторы в МНС:

Другие поля

Поле	Значение
Month	SEP-OCT
Publisher	ELSEVIER SCIENCE BV
Address	PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS
Language	English
EISSN	1364-551X
Keywords-Plus	N-ALKYLAZINIUM CATIONS; ONE-STEP ROUTE; CONDENSED 1,2,4-TRIAZINES; TANDEM A(N)-A(N); LIQUID-AMMONIA; NITRO-GROUP; DERIVATIVES; CHEMISTRY; AZINES; SALTS
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Multidisciplinary
Author-Email	charushin@htf.ustu.ru charushin@ios.uran.ru
Number-of-Cited-References	67
Usage-Count-Since-2013	6
Journal-ISO	Mendeleev Commun.
Doc-Delivery-Number	231JJ