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Volumn 624, Issue 1-2, 2001, Pages 367-371

Hydrosilylation of aldehydes and ketones catalyzed by [Ph3P(CuH)]6

Author keywords

Copper hydride; Hydrosilylation; Selective reductions; Silyl ethers

Indexed keywords


EID: 0001713466     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-328X(00)00903-7     Document Type: Article
Times cited : (94)

References (21)
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    • For some recent representative examples, see (a) N.J. Lawrence, S.M. Bushell, Tetrahedron Lett. 41 (2000) 4507. (b) D.J. Parks, J.M. Blackwell, W.E. Piers, J. Org. Chem. 65 (2000) 3090. (c) Y. Hu, J.A. Porco, Jr., Tetrahedron Lett. 39 (1998) 2711. (d) T. Ohkuma, S. Hashiguchi, R. Noyori, J. Org. Chem. 59 (1994) 217. (e) M. Fujita, T. Hiyama, J. Org. Chem. 53 (1988) 5405.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 4507
    • Lawrence, N.J.1    Bushell, S.M.2
  • 2
    • 0034685977 scopus 로고    scopus 로고
    • For some recent representative examples, see (a) N.J. Lawrence, S.M. Bushell, Tetrahedron Lett. 41 (2000) 4507. (b) D.J. Parks, J.M. Blackwell, W.E. Piers, J. Org. Chem. 65 (2000) 3090. (c) Y. Hu, J.A. Porco, Jr., Tetrahedron Lett. 39 (1998) 2711. (d) T. Ohkuma, S. Hashiguchi, R. Noyori, J. Org. Chem. 59 (1994) 217. (e) M. Fujita, T. Hiyama, J. Org. Chem. 53 (1988) 5405.
    • (2000) J. Org. Chem. , vol.65 , pp. 3090
    • Parks, D.J.1    Blackwell, J.M.2    Piers, W.E.3
  • 3
    • 0032580382 scopus 로고    scopus 로고
    • For some recent representative examples, see (a) N.J. Lawrence, S.M. Bushell, Tetrahedron Lett. 41 (2000) 4507. (b) D.J. Parks, J.M. Blackwell, W.E. Piers, J. Org. Chem. 65 (2000) 3090. (c) Y. Hu, J.A. Porco, Jr., Tetrahedron Lett. 39 (1998) 2711. (d) T. Ohkuma, S. Hashiguchi, R. Noyori, J. Org. Chem. 59 (1994) 217. (e) M. Fujita, T. Hiyama, J. Org. Chem. 53 (1988) 5405.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 2711
    • Hu, Y.1    Porco J.A., Jr.2
  • 4
    • 0028331228 scopus 로고
    • For some recent representative examples, see (a) N.J. Lawrence, S.M. Bushell, Tetrahedron Lett. 41 (2000) 4507. (b) D.J. Parks, J.M. Blackwell, W.E. Piers, J. Org. Chem. 65 (2000) 3090. (c) Y. Hu, J.A. Porco, Jr., Tetrahedron Lett. 39 (1998) 2711. (d) T. Ohkuma, S. Hashiguchi, R. Noyori, J. Org. Chem. 59 (1994) 217. (e) M. Fujita, T. Hiyama, J. Org. Chem. 53 (1988) 5405.
    • (1994) J. Org. Chem. , vol.59 , pp. 217
    • Ohkuma, T.1    Hashiguchi, S.2    Noyori, R.3
  • 5
    • 0000533235 scopus 로고
    • For some recent representative examples, see (a) N.J. Lawrence, S.M. Bushell, Tetrahedron Lett. 41 (2000) 4507. (b) D.J. Parks, J.M. Blackwell, W.E. Piers, J. Org. Chem. 65 (2000) 3090. (c) Y. Hu, J.A. Porco, Jr., Tetrahedron Lett. 39 (1998) 2711. (d) T. Ohkuma, S. Hashiguchi, R. Noyori, J. Org. Chem. 59 (1994) 217. (e) M. Fujita, T. Hiyama, J. Org. Chem. 53 (1988) 5405.
    • (1988) J. Org. Chem. , vol.53 , pp. 5405
    • Fujita, M.1    Hiyama, T.2
  • 7
    • 0345909313 scopus 로고
    • Protecting Groups, Thieme, Stuttgart
    • (b) P.J. Kocienski, Protecting Groups, Thieme, Stuttgart, 1994.
    • (1994)
    • Kocienski, P.J.1
  • 10
    • 0003944494 scopus 로고
    • R.J.K. Taylor (Ed.), Oxford University Press, Oxford
    • (a) I. Fleming, in: R.J.K. Taylor (Ed.), Organocopper Reagents, Oxford University Press, Oxford, 1994, p. 257.
    • (1994) Organocopper Reagents , pp. 257
    • Fleming, I.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.