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Volumn 135, Issue 24, 2013, Pages 9083-9090

Functional-group-tolerant, nickel-catalyzed cross-coupling reaction for enantioselective construction of tertiary methyl-bearing stereocenters

Author keywords

[No Author keywords available]

Indexed keywords

CROSS COUPLING REACTIONS; CROSS-COUPLINGS; DIRECTING GROUPS; ENANTIOSELECTIVE CONSTRUCTION; ENANTIOSELECTIVE SYNTHESIS; FATTY ACID AMIDE HYDROLASE; RETINOIC ACID RECEPTOR AGONISTS; STEREOSPECIFICITY;

EID: 84879383577     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja4034999     Document Type: Article
Times cited : (109)

References (92)
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    • For a review of general asymmetric cross-coupling strategies, see: Swift, E. C.; Jarvo, E. R. Tetrahedron 2013, DOI: 10.1016/j.tet.2013.05.001 (published online May 6, 2013).
    • (2013) Tetrahedron
    • Swift, E.C.1    Jarvo, E.R.2
  • 67
    • 0032541271 scopus 로고    scopus 로고
    • Alcohols prepared by the CBS reduction were assigned on the basis of the predictive model described in Corey, E. J.; Helal, C. J. Angew. Chem., Int. Ed. 1998, 37, 1986
    • (1998) Angew. Chem., Int. Ed. , vol.37 , pp. 1986
    • Corey, E.J.1    Helal, C.J.2
  • 74
    • 77956563162 scopus 로고    scopus 로고
    • Prodrugs and Drug Latentiation
    • In, 11 th ed. Block, J. H. Beale, J. M. Jr. Baltimore
    • Smith, F. T.; Clark, C. R. Prodrugs and Drug Latentiation. In Organic Medicinal and Pharmaceutical Chemistry, 11 th ed.; Block, J. H.; Beale, J. M., Jr., Eds.; Baltimore, 2004; pp 142.
    • (2004) Organic Medicinal and Pharmaceutical Chemistry , pp. 142
    • Smith, F.T.1    Clark, C.R.2
  • 82
    • 84894899083 scopus 로고    scopus 로고
    • See SI for full details. CCDC-940966 contains the supplemental crystallographic data for this structure. These data can be obtained free of charge from the Cambridge Crystallographic Data Center via www.ccdc.cam.ac.uk/ data-request/cif.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.