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Volumn 69, Issue 20, 2004, Pages 6572-6589

Preparation and resolution of a modular class of axially chiral quinazoline-containing ligands and their application in asymmetric rhodium-catalyzed olefin hydroboration

Author keywords

[No Author keywords available]

Indexed keywords

AMINES; CATALYST ACTIVITY; CATALYST SELECTIVITY; CHEMICAL BONDS; COMPLEXATION; CRYSTALLIZATION; OLEFINS; RHODIUM; SEPARATION; SYNTHESIS (CHEMICAL); X RAY CRYSTALLOGRAPHY;

EID: 4644223893     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo049195+     Document Type: Article
Times cited : (104)

References (63)
  • 45
    • 4644329739 scopus 로고    scopus 로고
    • note
    • Freshly distilled substrate and catecholborane were used for optimum catalytic performance.
  • 46
    • 4644346009 scopus 로고    scopus 로고
    • note
    • The hydroboration of styrene with both Quinazolinap- and Quinap-derived rhodium complexes was complete after 2 h at ambient temperature, whereas an extended reaction time of 12 h was necessary for complete reaction with Pyphos at this temperature.
  • 47
    • 4644270792 scopus 로고    scopus 로고
    • note
    • Regioselectivities of 97:3 and 99:1 were obtained with Quinap and Pyphos, respectively.
  • 49
    • 4644358652 scopus 로고    scopus 로고
    • Bristol-Myers Co. Patent DE 1806169; Chem. Abstr. 1970, 72
    • Bristol-Myers Co. Patent DE 1806169; Chem. Abstr. 1970, 72.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.