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Volumn 8, Issue 1, 2006, Pages 171-174

Theory-guided discovery of unique chemical transformations of cyclopropenes

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EID: 30944454327     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol052752+     Document Type: Article
Times cited : (53)

References (39)
  • 6
    • 1842450538 scopus 로고    scopus 로고
    • For an outstanding exposition of strain energies in unsaturated cyclopropanes and their origins, see: Bach, R. D.; Dmitrenko, O. J. Am. Chem. Soc. 2004, 126, 4444-4452.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 4444-4452
    • Bach, R.D.1    Dmitrenko, O.2
  • 7
    • 3242778811 scopus 로고    scopus 로고
    • Houben-Weyl; Thieme: Stuttgart
    • For recent reviews of transformations on cyclopropenes, see: (a) Baird, M. S. Cyclopropanes: Synthesis: From Cyclopropenes. In Houben-Weyl; Thieme: Stuttgart, 1997; pp 114-255.
    • (1997) Cyclopropanes: Synthesis: from Cyclopropenes , pp. 114-255
    • Baird, M.S.1
  • 12
    • 30944437481 scopus 로고    scopus 로고
    • For full details, see Supporting Information
    • For full details, see Supporting Information.
  • 21
    • 2042427265 scopus 로고
    • For C-C cleavage as a consequence of the high strain energy of 2-cyclopropenols, see: Wolff, S.; Agosta, W. C. J. Am. Chem. Soc. 1984, 106, 2363-2367.
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 2363-2367
    • Wolff, S.1    Agosta, W.C.2
  • 31
    • 30944446880 scopus 로고
    • Lloyd, D., Ed.; Plenum: New York
    • (j) Lloyd, D. In Topics in Carbocyclic Chemistry; Lloyd, D., Ed.; Plenum: New York, 1969; Vol. 1, pp 249-268.
    • (1969) Topics in Carbocyclic Chemistry , vol.1 , pp. 249-268
    • Lloyd, D.1
  • 35
    • 0006513782 scopus 로고
    • In general, methodology for the highly enantioselective synthesis of methylenecyclopropanes is poorly developed. See: (a) Lautens, M.; Delanghe, P. H. M. J. Org. Chem. 1993, 58, 5037-5039.
    • (1993) J. Org. Chem. , vol.58 , pp. 5037-5039
    • Lautens, M.1    Delanghe, P.H.M.2
  • 39
    • 30944438516 scopus 로고    scopus 로고
    • note
    • Approximately 9% of the cis-isomer of Feist's mono ester 21 was produced in the carboxylation of 20. This cis impurity was removed by silica gel chromatography after conversion to the diester 22.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.