메뉴 건너뛰기




Volumn , Issue 6, 1997, Pages 799-800

Lithium tri-tert-butylzincate as a chemoselective metallating reagent for functionalized organic halides

Author keywords

[No Author keywords available]

Indexed keywords


EID: 33748663073     PISSN: 0300922X     EISSN: None     Source Type: Journal    
DOI: 10.1039/a608294g     Document Type: Article
Times cited : (41)

References (29)
  • 21
    • 0028075131 scopus 로고
    • For a recent example of the use of the tert-butyl group as a nontransfer group, see E. Laloe and M. Srebnik, Tetrahedron Lett., 1994, 35, 5587.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 5587
    • Laloe, E.1    Srebnik, M.2
  • 22
    • 33748670972 scopus 로고    scopus 로고
    • LTBZ has been used for halogen-zinc exchanges; however no advantage as a selective metallating reagent has been demonstrated. See ref. 2(f), (g), (h)
    • LTBZ has been used for halogen-zinc exchanges; however no advantage as a selective metallating reagent has been demonstrated. See ref. 2(f), (g), (h).
  • 28
    • 0001689797 scopus 로고
    • Reformatsky type organozinc derivatives have been prepared via an oxidative addition reaction of functionalized alkyl halides to zinc. See M. W. Rathke, Org. React., 1975, 22, 423.
    • (1975) Org. React. , vol.22 , pp. 423
    • Rathke, M.W.1
  • 29
    • 0028575490 scopus 로고
    • Some examples of similar types of transmetallation have been reported. See: B. H. Lipshutz and M. R. Wood, J. Am. Chem. Soc., 1994, 116, 11 689 and references cited therein.
    • (1994) J. Am. Chem. Soc. , vol.116 , Issue.11 , pp. 689
    • Lipshutz, B.H.1    Wood, M.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.