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Volumn 15, Issue 16, 2013, Pages 4102-4105

Reductive cleavage of aryl O-carbamates to phenols by the Schwartz reagent. Expedient link to the directed ortho metalation strategy‡

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EID: 84882757378     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol401547d     Document Type: Article
Times cited : (29)

References (23)
  • 3
    • 22244435422 scopus 로고    scopus 로고
    • Rappoport, Z. Marek, I. Wiley: Chichester
    • Clayden, J. In Chemistry of Organolithium Compounds; Rappoport, Z., Marek, I., Eds.; Wiley: Chichester, 2004; Vol. 1, p 495.
    • (2004) Chemistry of Organolithium Compounds , vol.1 , pp. 495
    • Clayden, J.1
  • 12
    • 84882745270 scopus 로고    scopus 로고
    • M.Sc. Thesis, Queen's University, Kingston, ON, Canada
    • Morin, J. M.Sc. Thesis, Queen's University, Kingston, ON, Canada, 2007.
    • (2007)
    • Morin, J.1
  • 16
    • 84882780452 scopus 로고    scopus 로고
    • See Supporting Information
    • See Supporting Information.
  • 20
    • 84882755686 scopus 로고
    • Electrophilic bromination affords either 1-bromo or 1,6-dibromo 2-naphthols; see: Koelsch, C. F. Org. Synth. 1955, 20, 18
    • (1955) Org. Synth. , vol.20 , pp. 18
    • Koelsch, C.F.1
  • 21
    • 84882779791 scopus 로고    scopus 로고
    • Ph.D. Thesis, Queen's Univesity, Kingston, ON, Canada
    • Zhao, Y. Ph.D. Thesis, Queen's Univesity, Kingston, ON, Canada, 2010.
    • (2010)
    • Zhao, Y.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.