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Volumn 624, Issue 1-2, 2001, Pages 5-17

Carbon nucleophile addition to sp2-unsaturated Fischer carbene complexes

Author keywords

Asymmetric synthesis; Carbon nucleophilic addition; Fischer carbene complexes

Indexed keywords


EID: 0002829592     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-328X(00)00837-8     Document Type: Article
Times cited : (107)

References (68)
  • 4
    • 0000533326 scopus 로고
    • B.M. Trost, I. Fleming (Eds.), Pergamon, New York
    • (c) W.D. Wulff, in: B.M. Trost, I. Fleming (Eds.), Comprehensive Organic Synthesis, vol. 5, Pergamon, New York, 1991, p. 1065.
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 1065
    • Wulff, W.D.1
  • 5
    • 0000134379 scopus 로고
    • E.W. Abel, F.G.A. Stone, G. Wilkinson (Eds.), Pergamon, Oxford
    • (d) M.P. Doyle, in: E.W. Abel, F.G.A. Stone, G. Wilkinson (Eds.), Comprehensive Organometallic Chemistry II, vol. 12, Pergamon, Oxford, 1995, p. 387.
    • (1995) Comprehensive Organometallic Chemistry II , vol.12 , pp. 387
    • Doyle, M.P.1
  • 6
    • 0000134377 scopus 로고
    • E.W. Abel, F.G.A. Stone, G. Wilkinson (Eds.), Pergamon, Oxford
    • (e) W.D. Wulff, in: E.W. Abel, F.G.A. Stone, G. Wilkinson (Eds.), Comprehensive Organometallic Chemistry II, vol. 12, Pergamon, Oxford, 1995, p. 469.
    • (1995) Comprehensive Organometallic Chemistry II , vol.12 , pp. 469
    • Wulff, W.D.1
  • 7
    • 0000951659 scopus 로고
    • E.W. Abel, F.G.A. Stone, G. Wilkinson (Eds.), Pergamon, Oxford
    • (f) L.S. Hegedus, in: E.W. Abel, F.G.A. Stone, G. Wilkinson (Eds.), Comprehensive Organometallic Chemistry II, vol. 12, Pergamon, Oxford, 1995, p. 549.
    • (1995) Comprehensive Organometallic Chemistry II , vol.12 , pp. 549
    • Hegedus, L.S.1
  • 38
    • 37049092519 scopus 로고
    • These reactive dilithium dianions were prepared from the corresponding chlorohydrins; see: (a) J. Barluenga, J. Flórez, M. Yus, J. Chem. Soc. Chem. Commun. (1982) 1153. (b) J. Barluenga, J. Flórez, M. Yus, J. Chem. Soc. Perkin Trans. 1 (1983) 3019. (c) C. Nájera, M. Yus, D. Seebach, Helv. Chim. Acta 67 (1984) 289. (d) M. Yus, D.J. Ramón, J. Chem. Soc. Chem. Commun. (1991) 398.
    • (1982) J. Chem. Soc. Chem. Commun. , pp. 1153
    • Barluenga, J.1    Flórez, J.2    Yus, M.3
  • 39
    • 37049095951 scopus 로고
    • These reactive dilithium dianions were prepared from the corresponding chlorohydrins; see: (a) J. Barluenga, J. Flórez, M. Yus, J. Chem. Soc. Chem. Commun. (1982) 1153. (b) J. Barluenga, J. Flórez, M. Yus, J. Chem. Soc. Perkin Trans. 1 (1983) 3019. (c) C. Nájera, M. Yus, D. Seebach, Helv. Chim. Acta 67 (1984) 289. (d) M. Yus, D.J. Ramón, J. Chem. Soc. Chem. Commun. (1991) 398.
    • (1983) J. Chem. Soc. Perkin Trans. 1 , pp. 3019
    • Barluenga, J.1    Flórez, J.2    Yus, M.3
  • 40
    • 84986409746 scopus 로고
    • These reactive dilithium dianions were prepared from the corresponding chlorohydrins; see: (a) J. Barluenga, J. Flórez, M. Yus, J. Chem. Soc. Chem. Commun. (1982) 1153. (b) J. Barluenga, J. Flórez, M. Yus, J. Chem. Soc. Perkin Trans. 1 (1983) 3019. (c) C. Nájera, M. Yus, D. Seebach, Helv. Chim. Acta 67 (1984) 289. (d) M. Yus, D.J. Ramón, J. Chem. Soc. Chem. Commun. (1991) 398.
    • (1984) Helv. Chim. Acta , vol.67 , pp. 289
    • Nájera, C.1    Yus, M.2    Seebach, D.3
  • 41
    • 37049073704 scopus 로고
    • These reactive dilithium dianions were prepared from the corresponding chlorohydrins; see: (a) J. Barluenga, J. Flórez, M. Yus, J. Chem. Soc. Chem. Commun. (1982) 1153. (b) J. Barluenga, J. Flórez, M. Yus, J. Chem. Soc. Perkin Trans. 1 (1983) 3019. (c) C. Nájera, M. Yus, D. Seebach, Helv. Chim. Acta 67 (1984) 289. (d) M. Yus, D.J. Ramón, J. Chem. Soc. Chem. Commun. (1991) 398.
    • (1991) J. Chem. Soc. Chem. Commun. , pp. 398
    • Yus, M.1    Ramón, D.J.2
  • 54
    • 0347172435 scopus 로고    scopus 로고
    • note
    • For a recent paper where the alkenyl metallic species, generated by 1,4-addition of ketone, ester, or amide lithium enolates to tungsten alkenylcarbene complexes, are oxidized with iodine, see Ref. [19].
  • 64
    • 0012371956 scopus 로고
    • For preliminary reactions of α-carbene complex anions with alkenylcarbene complexes in which either the latter or the former component were, respectively, generated in situ under the reaction conditions, see: (a) C.P. Casey, W.R. Brunsvold, J. Organomet. Chem. 102 (1975) 175. (b) D.W. Macomber, M.-H. Hung, J. Organomet. Chem. 366 (1989) 147.
    • (1975) J. Organomet. Chem. , vol.102 , pp. 175
    • Casey, C.P.1    Brunsvold, W.R.2
  • 65
    • 0343821951 scopus 로고
    • For preliminary reactions of α-carbene complex anions with alkenylcarbene complexes in which either the latter or the former component were, respectively, generated in situ under the reaction conditions, see: (a) C.P. Casey, W.R. Brunsvold, J. Organomet. Chem. 102 (1975) 175. (b) D.W. Macomber, M.-H. Hung, J. Organomet. Chem. 366 (1989) 147.
    • (1989) J. Organomet. Chem. , vol.366 , pp. 147
    • Macomber, D.W.1    Hung, M.-H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.