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Titolo:
Alkylindan synthesis via an intermolecular [3+2] cycloaddition between unactivated alkenes and in situ generated p-quinomethanes
Autore:
Kim, S; Kitano, Y; Tada, M; Chiba, K;
Indirizzi:
Tokyo Univ Agr & Technol, Bioorgan Chem Lab, Fuchu, Tokyo 1838509, Japan Tokyo Univ Agr & Technol Fuchu Tokyo Japan 1838509 , Tokyo 1838509, Japan
Titolo Testata:
TETRAHEDRON LETTERS
fascicolo: 36, volume: 41, anno: 2000,
pagine: 7079 - 7083
SICI:
0040-4039(20000902)41:36<7079:ASVAI[>2.0.ZU;2-W
Fonte:
ISI
Lingua:
ENG
Soggetto:
O-QUINONE METHIDES; ELECTROCHEMICAL OXIDATION; EUGLOBAL SKELETONS; REACTIVITY; CHROMANS;
Keywords:
addition reactions; cyclization; indanes/hydrindane; phenols;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Life Sciences
Physical, Chemical & Earth Sciences
Citazioni:
24
Recensione:
Indirizzi per estratti:
Indirizzo: Chiba, K Tokyo Univ Agr & Technol, Bioorgan Chem Lab, 3-5-8 Saiwai Cho, Fuchu, Tokyo 1838509, Japan Tokyo Univ Agr & Technol 3-5-8 Saiwai Cho Fuchu Tokyo Japan 1838509
Citazione:
S. Kim et al., "Alkylindan synthesis via an intermolecular [3+2] cycloaddition between unactivated alkenes and in situ generated p-quinomethanes", TETRAHEDR L, 41(36), 2000, pp. 7079-7083

Abstract

Alkylindans were synthesized by the intermolecular [3+2] cycloaddition of in situ generated p-quinomethanes and aliphatic alkenes. In a highly concentrated lithium perchlorate in nitromethane, p-quinomethanes were generated by DDQ oxidation of corresponding alkylphenols, and the desired cycloaddition reaction was completed efficiently to give various indans. (C) 2000 Elsevier Science Ltd. All rights reserved.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 01/10/20 alle ore 04:18:53