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Volumn 355, Issue 14-15, 2013, Pages 2900-2907

Practical asymmetric catalytic synthesis of spiroketals and chiral diphosphine ligands

Author keywords

Asymmetric catalysis; Diphosphine li gands; Hydrogenation; Iridium; Spiroketals

Indexed keywords


EID: 84892140547     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201300380     Document Type: Article
Times cited : (68)

References (93)
  • 54
    • 84858257928 scopus 로고    scopus 로고
    • a) I. Coric, B. List, Nature 2012, 483, 315. For a highlight of the works reported in refs.[10,11a];
    • (2012) Nature , vol.483 , pp. 315
    • Coric, I.1    List, B.2
  • 65
    • 84891564839 scopus 로고    scopus 로고
    • Wiley-VCH, Weinheim
    • The spiro backbone has been recognized as a privileged structure for the construction of chiral ligands; see: a) Privileged Chiral Ligands and Catalysts, (Ed. : Q.-L. Zhou), Wiley-VCH, Weinheim, 2011;
    • (2011) Privileged Chiral Ligands and Catalysts
    • Zhou, Q.-L.1
  • 77
    • 84987590261 scopus 로고
    • For examples of transition metal complex-catalyzed acetalizations, see: f) F. Gorla, L. M. Venanzi, Helv. Chim. Acta 1990, 73, 690;
    • (1990) Helv. Chim. Acta , vol.73 , pp. 690
    • Gorla, F.1    Venanzi, L.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.