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Volumn 77, Issue 14, 2012, Pages 6208-6214

Enantioselective synthesis of trans -dihydrobenzofurans via primary amine-thiourea organocatalyzed intramolecular michael addition

Author keywords

[No Author keywords available]

Indexed keywords

DIHYDROBENZOFURANS; ENANTIOSELECTIVE SYNTHESIS; HIGH TEMPERATURE; HIGH YIELD; IN-SITU; INTRAMOLECULAR MICHAEL ADDITION;

EID: 84864053226     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo301006e     Document Type: Article
Times cited : (67)

References (66)
  • 36
    • 80051716582 scopus 로고    scopus 로고
    • Examples of organocatalytic asymmetric intramolecular Michael addition and the related reactions, see
    • Examples of organocatalytic asymmetric intramolecular Michael addition and the related reactions, see: Moyano, A.; Rios, R. Chem. Rev. 2011, 111, 4703
    • (2011) Chem. Rev. , vol.111 , pp. 4703
    • Moyano, A.1    Rios, R.2
  • 63
    • 81755183021 scopus 로고    scopus 로고
    • An example of enantioselective protonation of branched aldehydes through enamine intermediates, see
    • An example of enantioselective protonation of branched aldehydes through enamine intermediates, see: Fu, N.; Zhang, L.; Li, J.; Luo, S.; Cheng, J.-P. Angew. Chem., Int. Ed. 2011, 50, 11451
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 11451
    • Fu, N.1    Zhang, L.2    Li, J.3    Luo, S.4    Cheng, J.-P.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.