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Titolo:
Synthesis of bridged analogs of epibatidine. 3-chloro-5,7,8,9,9a,10-hexahydro-7,10-methanopyrrolo[1,2-b]-2,6-naphthyridine and 2-chloro-5,5a,6,7,8,10-hexahydro-5,8-methanopyrrolo[2,1-b]-1,7-naphthyridine
Autore:
Brieaddy, LE; Mascarella, SW; Navarro, HA; Atkinson, RN; Damaj, MI; Martin, BR; Carroll, FI;
Indirizzi:
Res Triangle Inst, Res Triangle Pk, NC 27709 USA Res Triangle Inst Res Triangle Pk NC USA 27709 Triangle Pk, NC 27709 USA Virginia Commonwealth Univ, Coll Med, Dept Pharmacol & Toxicol, Richmond, VA 23298 USA Virginia Commonwealth Univ Richmond VA USA 23298 , Richmond, VA 23298 USA
Titolo Testata:
TETRAHEDRON LETTERS
fascicolo: 23, volume: 42, anno: 2001,
pagine: 3795 - 3797
SICI:
0040-4039(20010604)42:23<3795:SOBAOE>2.0.ZU;2-A
Fonte:
ISI
Lingua:
ENG
Soggetto:
NICOTINIC ACETYLCHOLINE-RECEPTORS; TARGETS;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Life Sciences
Physical, Chemical & Earth Sciences
Citazioni:
22
Recensione:
Indirizzi per estratti:
Indirizzo: Carroll, FI Res Triangle Inst, POB 12194, Res Triangle Pk, NC 27709 USA Res Triangle Inst POB 12194 Res Triangle Pk NC USA 27709 9 USA
Citazione:
L.E. Brieaddy et al., "Synthesis of bridged analogs of epibatidine. 3-chloro-5,7,8,9,9a,10-hexahydro-7,10-methanopyrrolo[1,2-b]-2,6-naphthyridine and 2-chloro-5,5a,6,7,8,10-hexahydro-5,8-methanopyrrolo[2,1-b]-1,7-naphthyridine", TETRAHEDR L, 42(23), 2001, pp. 3795-3797

Abstract

The synthesis of conformationally locked analogs of epibatidine are described in which the key step is an intramolecular reductive palladium-catalyzed Heck-type coupling. (C) 2001 Elsevier Science Ltd. All rights reserved.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 22/09/20 alle ore 16:43:26