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Volumn 7, Issue 12, 2001, Pages 2671-2675

Mechanism of 1,6-addition reactions of organocuprates: Detailed NMR spectroscopic study of a cuprate - Enyne π complex

Author keywords

Cuprates; Enynes; NMR spectroscopy; pi complexes

Indexed keywords

ALKENE; CARBON 13; COPPER COMPLEX;

EID: 0035907847     PISSN: 09476539     EISSN: None     Source Type: Journal    
DOI: 10.1002/1521-3765(20010618)7:12<2671::AID-CHEM26710>3.0.CO;2-S     Document Type: Article
Times cited : (22)

References (32)
  • 1
    • 0000175697 scopus 로고
    • (Ed.: Y. Yamamoto), Thieme, Stuttgart
    • a) Y. Yamamoto in Stereoselective Syntheses, Vol. 4 (Ed.: Y. Yamamoto), Thieme, Stuttgart, 1995, pp. 2041-2057;
    • (1995) Stereoselective Syntheses , vol.4 , pp. 2041-2057
    • Yamamoto, Y.1
  • 24
    • 0000283131 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 3750-3771.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 3750-3771
  • 26
    • 85037325486 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 1999, 35, 1644-1646.
    • (1999) Angew. Chem. Int. Ed. , vol.35 , pp. 1644-1646
  • 29
    • 0030910107 scopus 로고    scopus 로고
    • [6a] and experimental studies (determination of kinetic isotope effects: D. E. Frantz, D. A. Singleton, J. P. Snyder, J. Am. Chem. Soc. 1997, 119, 3383-3384) indicate that the reductive elimination of a copper(III) species is the rate-determining step. Analogous investigations have not been carried out to date for the 1,6-addition to acceptor-substituted enynes.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 3383-3384
    • Frantz, D.E.1    Singleton, D.A.2    Snyder, J.P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.