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Volumn 14, Issue 18, 2012, Pages 4758-4761

Enantioselective synthesis of 2,6-cis-disubstituted tetrahydropyrans via a tandem catalytic asymmetric hydrogenation/oxa-Michael cyclization: An efficient approach to (-)-centrolobine

Author keywords

[No Author keywords available]

Indexed keywords

CENTROLOBIN; PYRAN DERIVATIVE;

EID: 84868248664     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol3020144     Document Type: Article
Times cited : (43)

References (53)
  • 10
    • 39149102146 scopus 로고    scopus 로고
    • For recent reviews including the synthesis of tetrahydropyrans, see: (a) Larrosa, I.; Romea, P.; Urpí, F. Tetrahedron 2008, 64, 2683.
    • (2008) Tetrahedron , vol.64 , pp. 2683
    • Larrosa, I.1    Romea, P.2    Urpí, F.3
  • 14
  • 15
    • 79952264446 scopus 로고    scopus 로고
    • For selected recent papers including creation of chiral cis-2,6- tetrahydropyrans via oxa-Michael cyclization, see: (a) Kanematsu, M.; Yoshida, M.; Shishido, K. Angew. Chem., Int. Ed. 2011, 50, 2618.
    • (2011) Angew. Chem., Int. Ed. , vol.50 , pp. 2618
    • Kanematsu, M.1    Yoshida, M.2    Shishido, K.3
  • 26
    • 84891035198 scopus 로고    scopus 로고
    • de Vries, J. G., Elsevier, C. J., Eds.; Wiley-VCH: Weinheim
    • Ohkuma, T.; Noyori, R. In Handbook of Homogeneous Hydrogenation, Vol. 3; de Vries, J. G., Elsevier, C. J., Eds.; Wiley-VCH: Weinheim, 2007; p 1105.
    • (2007) Handbook of Homogeneous Hydrogenation , vol.3 , pp. 1105
    • Ohkuma, T.1    Noyori, R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.