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Volumn , Issue 13, 2011, Pages 2417-2420

Intermolecular amination of allyl alcohols with sulfamates: Effective utilization of mercuric catalyst

Author keywords

Allylation; Amination; Mercury; Sulfur; Supported catalysts

Indexed keywords


EID: 79954590469     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.201100054     Document Type: Article
Times cited : (20)

References (39)
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    • Recent reports on Tsuji-Trost-type allylic amination
    • Recent reports on Tsuji-Trost-type allylic amination
  • 10
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    • Recent review on the Tsuji-Trost-type reaction of allylic alcohols
    • Recent review on the Tsuji-Trost-type reaction of allylic alcohols
  • 11
  • 13
    • 79954586741 scopus 로고    scopus 로고
    • Recent reports on the direct allylic amination of allylic alcohols
    • Recent reports on the direct allylic amination of allylic alcohols
  • 20
    • 79954618589 scopus 로고    scopus 로고
    • H. Yamamoto, E. Ho, I. Sasaki, M. Mitsutake, Y. Takagi, H. Imagawa, M. Nishizawa, unpublished results (cf. Supporting Information)
    • H. Yamamoto, E. Ho, I. Sasaki, M. Mitsutake, Y. Takagi, H. Imagawa, M. Nishizawa, unpublished results (cf. Supporting Information).
  • 23
    • 79954588248 scopus 로고    scopus 로고
    • Recent reports on the reaction using sulfamate derivatives
    • Recent reports on the reaction using sulfamate derivatives
  • 28
    • 71949117041 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2009, 48, 2777
    • T. Kurokawa, M. Kim, J. Du Bois, Angew. Chem. 2009, 121, 2815; Angew. Chem. Int. Ed. 2009, 48, 2777.
    • (2009) Angew. Chem. , vol.121 , pp. 2815
    • Kurokawa, T.1    Kim, M.2    Du Bois, J.3
  • 34
    • 79954600375 scopus 로고    scopus 로고
    • When optically active alcohol 5 (97%âee) and 7a were used, racemic product 8a was obtained
    • When optically active alcohol 5 (97%âee) and 7a were used, racemic product 8a was obtained.
  • 35
    • 79954610129 scopus 로고    scopus 로고
    • 2 catalytic conditions (cf. Supporting Information, pilot study-3)
    • 2 catalytic conditions (cf. Supporting Information, pilot study-3).
  • 36
    • 79954608269 scopus 로고    scopus 로고
    • Derivative 12 is unstable under acidic conditions. During column chromatography on silica gel 12 decomposed into 14
    • Derivative 12 is unstable under acidic conditions. During column chromatography on silica gel 12 decomposed into 14.
  • 37
    • 79954598397 scopus 로고    scopus 로고
    • The relative stereochemistry of tert-butyl ester 16 was established by NOESY experiments (cf. Supporting Information)
    • The relative stereochemistry of tert-butyl ester 16 was established by NOESY experiments (cf. Supporting Information).
  • 39
    • 79954604089 scopus 로고    scopus 로고
    • Note
    • The catalytic activity of recovered 17 was investigated by analyzing the same reaction of 5 with 7a to give 8a. The recycled catalyst displayed complete catalytic activity until the fourth reaction. However, a longer reaction time was required for the fifth reaction (cf. Supporting Information).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.