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Volumn 355, Issue 11-12, 2013, Pages 2139-2144

Atropodiastereoselective C-H olefination of biphenyl p-tolyl sulfoxides with acrylates

Author keywords

Axial chirality; Biaryls; C H functionalization; Olefination; Sulfoxides

Indexed keywords


EID: 84884503325     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201300446     Document Type: Article
Times cited : (130)

References (62)
  • 40
    • 0000297657 scopus 로고    scopus 로고
    • (Eds.: C. Scolastico, F. Nicotra), Plenum Publishing Corporation, New York
    • h) G. Bringmann, S. Tasler, in: Current Trends in Organic Synthesis, (Eds.: C. Scolastico, F. Nicotra), Plenum Publishing Corporation, New York, 1999, pp 105
    • (1999) Current Trends in Organic Synthesis , pp. 105
    • Bringmann, G.1    Tasler, S.2
  • 61
    • 84884502637 scopus 로고    scopus 로고
    • CCDC 928824 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC 928824 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
  • 62
    • 84884498536 scopus 로고    scopus 로고
    • 1H NMR experiments at high temprature showed that the coupling products 2b-i are atropoconfigurationnaly stable up to at least 100 8C.
    • 1H NMR experiments at high temprature showed that the coupling products 2b-i are atropoconfigurationnaly stable up to at least 100 8C.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.