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Volumn 39, Issue 40, 1998, Pages 7259-7262

Regioselective opening of substituted (cyclopropylmethyl)lithiums derived from cyclopropylmethyl iodides

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPROPANE DERIVATIVE; LITHIUM DERIVATIVE; METHANOL DERIVATIVE; METHYL IODIDE;

EID: 0032190812     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)01582-2     Document Type: Article
Times cited : (33)

References (25)
  • 7
    • 0010394316 scopus 로고
    • Rappoport, Z. Ed.; Wiley: New York; Chapter 8
    • 2. For reviews on the opening of cyclopropanes, see: (a) Ressig, H.-U. In The chemistry of the cyclopropyl group; Rappoport, Z. Ed.; Wiley: New York, 1987; Chapter 8.
    • (1987) The Chemistry of the Cyclopropyl Group
    • Ressig, H.-U.1
  • 9
    • 0009498652 scopus 로고
    • 3. For specific examples of ring opening of cyclopropanylmethanol derivatives, see: (a) Collum, D. B.; Still, W. C.; Mohamadi, F. J. Am. Chem. Soc. 1986, 108, 2094-2096.
    • (1986) J. Am. Chem. Soc. , vol.108 , pp. 2094-2096
    • Collum, D.B.1    Still, W.C.2    Mohamadi, F.3
  • 13
    • 33845556253 scopus 로고
    • 5. We found that these conditions were much more reliable with substituted cyclopropanes and afforded higher yields of the desired product that those used to prepare cyclopropylmethyl iodide: (a) Sieh, D. H.; Michejda, C. J. J. Am. Chem. Soc. 1981, 103, 442-445.
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 442-445
    • Sieh, D.H.1    Michejda, C.J.2
  • 16
    • 0000014060 scopus 로고
    • 6. For a seminal study of the opening of cyclopropylmethyl Grignard reagents, see: (a) Roberts, J. D.; Mazur, R. H. J. Am. Chem. Soc. 1951, 73, 2509-2520.
    • (1951) J. Am. Chem. Soc. , vol.73 , pp. 2509-2520
    • Roberts, J.D.1    Mazur, R.H.2
  • 20
    • 85038550328 scopus 로고    scopus 로고
    • note
    • 13C NMR, IR and HRMS and/or elemental analysis.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.