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Volumn 135, Issue 17, 2013, Pages 6419-6422

Catalytic, enantioselective, intramolecular carbosulfenylation of olefins

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC NUCLEOPHILES; ARYL-SUBSTITUTED ALKENES; ENANTIOMERIC RATIO; ENANTIOSELECTIVE; TETRAHYDRONAPHTHALENES;

EID: 84877082727     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja401867b     Document Type: Article
Times cited : (87)

References (46)
  • 1
    • 84877052395 scopus 로고
    • In, 2 nd ed. de la Mare, P. B. D. and Bolton, R. Eds. Elsevier: Amsterdam, Vol.
    • de la Mare, P. B. D. and Bolton, R. In Electrophilic Additions to Unsaturated Systems, 2 nd ed.; de la Mare, P. B. D. and Bolton, R., Eds. Elsevier: Amsterdam, 1982; Vol. 9, pp 198-246.
    • (1982) Electrophilic Additions to Unsaturated Systems , vol.9 , pp. 198-246
    • De La Mare, P.B.D.1    Bolton, R.2
  • 43
    • 84862812892 scopus 로고    scopus 로고
    • For a report of catalytic, enantioselective oxysulfenylation of unactivated alkenes under chiral Brønsted acid catalysis, see: Guan, H.; Wang, H.; Huang, D.; Shi, Y. Tetrahedron 2012, 68, 2728-2735
    • (2012) Tetrahedron , vol.68 , pp. 2728-2735
    • Guan, H.1    Wang, H.2    Huang, D.3    Shi, Y.4
  • 46
    • 84877073995 scopus 로고    scopus 로고
    • 1H NMR chemical shifts of HC(3) with known products trans - 2a and cis - 2a.(6, 18) The absolute configuration of (-)- trans - 3k was determined to be (1 R,2 R) by X-ray crystallographic analysis of the derived sulfone trans - 12. The crystallographic coordinates of trans - 12 have been deposited with the Cambridge Crystallographic Data Centre; deposition no. 913987. These data can be obtained free of charge via from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK; fax: (+44) 1223-336-033; via or deposit@ccdc.cam.ac.uk.
    • 1H NMR chemical shifts of HC(3) with known products trans-2a and cis-2a.(6, 18) The absolute configuration of (-)- trans-3k was determined to be (1 R,2 R) by X-ray crystallographic analysis of the derived sulfone trans-12. The crystallographic coordinates of trans-12 have been deposited with the Cambridge Crystallographic Data Centre; deposition no. 913987. These data can be obtained free of charge via from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK; fax: (+44) 1223-336-033; via www.ccdc.cam.ac.uk/conts/retrieving.html or deposit@ccdc.cam.ac.uk.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.