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Volumn , Issue 12, 2000, Pages 1785-1805

The control of remote asymmetric centres via reduction of acyclic carbonyl functions

Author keywords

[No Author keywords available]

Indexed keywords

CARBONYLATION; COMPLEXATION; ESTERS; HYDRIDES; KETONES; REDUCTION; SUBSTRATES; SYNTHESIS (CHEMICAL);

EID: 0034697712     PISSN: 14704358     EISSN: None     Source Type: Journal    
DOI: 10.1039/b000155o     Document Type: Article
Times cited : (35)

References (167)
  • 3
    • 0000046858 scopus 로고
    • ed. J. D. Morrison, Academic Press, New York
    • E. L. Eliel, in Asymmetric Synthesis, ed. J. D. Morrison, Academic Press, New York, 1983, vol. 2, p. 125;
    • (1983) Asymmetric Synthesis , vol.2 , pp. 125
    • Eliel, E.L.1
  • 6
    • 0000830285 scopus 로고    scopus 로고
    • For a review on strategies for stereoselective synthesis of molecules with remote stereogenic centres across a double bond of fixed configuration, see: H. J. Mitchell, A. Nelson and S. Warren, J. Chem. Soc., Perkin Trans, 1, 1999, 1899.
    • (1999) J. Chem. Soc., Perkin Trans, 1 , pp. 1899
    • Mitchell, H.J.1    Nelson, A.2    Warren, S.3
  • 7
    • 0032507927 scopus 로고    scopus 로고
    • For examples of l,>3-remote stereocontrol in direct additions to aldehydes, see: (a) T. Yoshida, J. Chika and H. Takei, Tetrahedron Lett., 1998, 39, 4305;
    • (1998) Tetrahedron Lett. , vol.39 , pp. 4305
    • Yoshida, T.1    Chika, J.2    Takei, H.3
  • 38
    • 0000765299 scopus 로고
    • For examples of remote stereocontrol in additions to acetals, see: ref. 4k; J. S. Panek and M. Yang, J. Am. Chem. Soc., 1991,113, 6594.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 6594
    • Panek, J.S.1    Yang, M.2
  • 39
  • 41
    • 0038106171 scopus 로고    scopus 로고
    • For examples of remote asymmetric induction in additions to imine derivatives, see: (a) R. Bloch, Chem. Rev., 1998, 98, 1407;
    • (1998) Chem. Rev. , vol.98 , pp. 1407
    • Bloch, R.1
  • 45
    • 0032552170 scopus 로고    scopus 로고
    • For an example of remote diastereocontrol in an electrophilic amination reaction, see: P. Arya, R. N. Ben and H. Qin, Tetrahedron Lett., 1998, 39, 6131.
    • (1998) Tetrahedron Lett. , vol.39 , pp. 6131
    • Arya, P.1    Ben, R.N.2    Qin, H.3
  • 46
  • 69
    • 0001840864 scopus 로고    scopus 로고
    • For examples of 1,>3-remote stereocontrol in C-alkylation reactions, see: refs. 10fand 11f; (a) D. J. Pippel, M. D. Curtis, H. Du and P. Beak, J. Org. Chem., 1998, 63, 2;
    • (1998) J. Org. Chem. , vol.63 , pp. 2
    • Pippel, D.J.1    Curtis, M.D.2    Du, H.3    Beak, P.4
  • 97
    • 0011165337 scopus 로고
    • For examples of 1,>3-stereocontrol in cyclic hydroboration reactions, see: (a) R. A. Whitney, Can. J. Chem., 1986, 64, 803;
    • (1986) Can. J. Chem. , vol.64 , pp. 803
    • Whitney, R.A.1
  • 99
    • 0027931792 scopus 로고
    • For examples of remote asymmetric induction in palladiumcatalysed cyclisation reactions, see: (a) K. Nordström and C. Moberg, Tetrahedron Lett., 1994, 35, 7267;
    • (1994) Tetrahedron Lett. , vol.35 , pp. 7267
    • Nordström, K.1    Moberg, C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.