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Volumn 17, Issue 10, 2015, Pages 2408-2411

Diastereoselective and Enantioselective Silylation of 2-Arylcyclohexanols

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EID: 84929593652     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/acs.orglett.5b00919     Document Type: Article
Times cited : (34)

References (58)
  • 8
    • 0000308108 scopus 로고
    • Ernest, L.; Wilen, S. H., Eds.; John Wiley and Sons: New York
    • Kagan, H. B.; Fiaud, J. C. In Topics in Stereochemistry; Ernest, L.; Wilen, S. H., Eds.; John Wiley and Sons: New York, 1988; Vol. 18, p 249.
    • (1988) Topics in Stereochemistry , vol.18 , pp. 249
    • Kagan, H.B.1    Fiaud, J.C.2
  • 54
    • 84929601631 scopus 로고    scopus 로고
    • note
    • Kinetic resolution of 998 mg of the compound in Table 2, entry 1: s = 10 with 52% conversion and recovered alcohol with an er of 85:15.
  • 55
    • 84929601632 scopus 로고    scopus 로고
    • note
    • Conversions and selectivity factors are based on the ee of the recovered starting materials and products. Percent conversion = ees/(ees + eep) × 100% and s = ln[(1-C)(1-ees)]/ln[(1-C)(1 + ees)], where ees = ee of recovered starting material and eep = ee of product. See ref 3a.
  • 56
    • 84929601633 scopus 로고    scopus 로고
    • note
    • Selectivity factors are an average of two runs. Conversions are from a single run.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.