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Titolo:
A novel route to stereodefined cyclopropyl-substituted alkenes
Autore:
Zhou, SM; Deng, MZ;
Indirizzi:
Chinese Acad Sci, Shanghai Inst Organ Chem, Organomet Chem Lab, Shanghai 200032, Peoples R China Chinese Acad Sci Shanghai Peoples R China 200032 200032, Peoples R China
Titolo Testata:
TETRAHEDRON LETTERS
fascicolo: 20, volume: 41, anno: 2000,
pagine: 3951 - 3954
SICI:
0040-4039(20000521)41:20<3951:ANRTSC>2.0.ZU;2-Y
Fonte:
ISI
Lingua:
ENG
Soggetto:
CROSS-COUPLING REACTIONS; ACIDS; HALIDES; ESTERS;
Keywords:
cyclopropylboronic acid; cyclopropyl-substituted alkenes; cross-coupling; palladium;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Life Sciences
Physical, Chemical & Earth Sciences
Citazioni:
15
Recensione:
Indirizzi per estratti:
Indirizzo: Deng, MZ Chinese Acad Sci, Shanghai Inst Organ Chem, Organomet Chem Lab, 354 Fenglin Lu, Shanghai 200032, Peoples R China Chinese Acad Sci 354 Fenglin Lu Shanghai Peoples R China 200032
Citazione:
S.M. Zhou e M.Z. Deng, "A novel route to stereodefined cyclopropyl-substituted alkenes", TETRAHEDR L, 41(20), 2000, pp. 3951-3954

Abstract

The first Tl2CO3 or Ag2O assisted Suzuki-type cross-coupling of stereodefined cyclopropylboronic acids with haloalkenes without electron-drawing groups to give the corresponding stereodefined cyclopropyl-substituted alkenes in good yields is described. The configurations of both cyclopropyl and alkenyl functions were retained in the reaction. (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 31/03/20 alle ore 22:37:07