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Volumn 38, Issue 42, 1997, Pages 7349-7352

Magnesium promoted cyclopropanation reactions of allylic alcohols

Author keywords

Allylic alcohols; Carbenoids; Cyclopropanation; Grignard reagents; Magnesium

Indexed keywords

CYCLOPROPANE DERIVATIVE;

EID: 0030770654     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)10009-0     Document Type: Article
Times cited : (32)

References (50)
  • 1
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    • New address: Institut für Organische Chemie der RWTH Aachen, Prof.-Pirlet Str. 1, D-52056 Aachen, Germany. FAX: (int.) 241 8888 391; e-mail: Carsten.Bolm@RWTH-Aachen.de
    • New address: Institut für Organische Chemie der RWTH Aachen, Prof.-Pirlet Str. 1, D-52056 Aachen, Germany. FAX: (int.) 241 8888 391; e-mail: Carsten.Bolm@RWTH-Aachen.de
  • 3
    • 0342650610 scopus 로고    scopus 로고
    • in ref. 1a, p. 265
    • (b) For the synthesis of cyclopropanes via metal carbenoids see: Subramanian, L. R.; Zeller, K. -P. in ref. 1a, p. 265.
    • Subramanian, L.R.1    Zeller, K.-P.2
  • 4
    • 0037599887 scopus 로고    scopus 로고
    • Houben-Weyl, Eds.: Helmchen, G.; Hoffmann, R. W.; Mulzer, J.; Schaumann, E., E 21, Thieme, Stuttgart
    • (c) For stereoselective cyclopropanations of various kinds see: Reissig, H. -U. in Stereoselective Synthesis, Houben-Weyl, (Eds.: Helmchen, G.; Hoffmann, R. W.; Mulzer, J.; Schaumann, E.), E 21, Vol. 5, Thieme, Stuttgart, 1996, p. 3179.
    • (1996) Stereoselective Synthesis , vol.5 , pp. 3179
    • Reissig, H.-U.1
  • 8
    • 33748223805 scopus 로고
    • (c) Kozhushkov S. I.; Haumann, T.; Boese, R.; de Meijere, A. Angew. Chem. 1993, 105, 426; Angew. Chem. Int. Ed. Engl. 1993, 32, 401.
    • (1993) Angew. Chem. Int. Ed. Engl. , vol.32 , pp. 401
  • 13
    • 33748895937 scopus 로고
    • (g) Hirsch, A.; Lamparth, I.; Karfunkel, H. R. Angew. Chem. 1994, 106, 453; Angew. Chem. Int. Ed. Engl. 1994, 33, 437.
    • (1994) Angew. Chem. Int. Ed. Engl. , vol.33 , pp. 437
  • 42
    • 0001095629 scopus 로고
    • For earlier studies on the transfer of substituted methylene groups using other metals see: (a) Nishimura, J.; Kawabata, N.; Furukawa, J. Tetrahedron 1969, 25, 2647.
    • (1969) Tetrahedron , vol.25 , pp. 2647
    • Nishimura, J.1    Kawabata, N.2    Furukawa, J.3
  • 48
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    • (g) Charette, A. B.; Lemay, J. Angew. Chem. 1997, 104, 1163; Angew. Chem. Int. Ed. Engl. 1997, 36, 1090 and references therein.
    • (1997) Angew. Chem. , vol.104 , pp. 1163
    • Charette, A.B.1    Lemay, J.2
  • 49
    • 0030767994 scopus 로고    scopus 로고
    • and references therein
    • (g) Charette, A. B.; Lemay, J. Angew. Chem. 1997, 104, 1163; Angew. Chem. Int. Ed. Engl. 1997, 36, 1090 and references therein.
    • (1997) Angew. Chem. Int. Ed. Engl. , vol.36 , pp. 1090
  • 50
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    • note
    • 3/TMS) δ = 13.9, 22.3, 24.9, 26.3, 26.7, 27.3, 31.6, 66.8, 125.7, 127.9, 128.9, 138.5 ppm.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.