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Volumn 12, Issue 19, 2010, Pages 4332-4334

Palladium-catalyzed [4 + 2] cycloaddition of o-(silylmethyl)benzyl esters with ketones: An equivalent to oxo-diels-alder reaction of o-xylylenes

Author keywords

[No Author keywords available]

Indexed keywords

BENZENE; ESTER; KETONE; PALLADIUM; XYLENE;

EID: 77957145213     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol101792a     Document Type: Article
Times cited : (24)

References (31)
  • 1
    • 77957121221 scopus 로고    scopus 로고
    • Examples of biologically active isochromane compounds
    • Examples of biologically active isochromane compounds
  • 7
    • 77957129477 scopus 로고    scopus 로고
    • For reports on the intramolecular reactions, see
    • For reports on the intramolecular reactions, see
  • 10
    • 77957125500 scopus 로고    scopus 로고
    • For reports on the intermolecular reactions, see
    • For reports on the intermolecular reactions, see
  • 15
    • 77957168718 scopus 로고    scopus 로고
    • Oppolzer attempted the intramolecular oxo-Diels-Alder reaction of o -xylylene without an electron-donating group but obtained the desired product in only 25% yield; see
    • Oppolzer attempted the intramolecular oxo-Diels-Alder reaction of o -xylylene without an electron-donating group but obtained the desired product in only 25% yield; see
  • 19
    • 77957149011 scopus 로고    scopus 로고
    • DPPPent = 1,5-bis(diphenylphosphino)pentane
    • DPPPent = 1,5-bis(diphenylphosphino)pentane
  • 21
    • 77957155627 scopus 로고    scopus 로고
    • DPEphos = bis[2-(diphenylphosphino)phenyl] ether
    • DPEphos = bis[2-(diphenylphosphino)phenyl] ether
  • 29
    • 77957119852 scopus 로고    scopus 로고
    • The A values of the trifluoromethyl and alkoxycarbonyl groups indicate that the former is sterically bulkier than the latter; see
    • The A values of the trifluoromethyl and alkoxycarbonyl groups indicate that the former is sterically bulkier than the latter; see


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.