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Volumn 53, Issue 45, 2012, Pages 5981-5983

Asymmetric induction by helical poly(amino acid)s in cyanosilylation of aldehydes

Author keywords

Helix; Asymmetric induction; Cyanosilylation; Poly(amino acid)s; Polyleucine

Indexed keywords

ALDEHYDE; LEUCINE; POLYAMINOACID;

EID: 84867248919     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2012.07.034     Document Type: Article
Times cited : (16)

References (86)
  • 8
    • 38349109422 scopus 로고
    • Other examples of helical-PAA-catalyzed enantioselective reactions, see
    • Other examples of helical-PAA-catalyzed enantioselective reactions, see: K. Ueyanagi, and S. Inoue Makromol. Chem. 177 1976 2807
    • (1976) Makromol. Chem. , vol.177 , pp. 2807
    • Ueyanagi, K.1    Inoue, S.2
  • 10
    • 69549106327 scopus 로고    scopus 로고
    • For examples of enantioselective reactions with helical polymers, see
    • For examples of enantioselective reactions with helical polymers, see: G. Maayan, M.D. Ward, and K. Kirshenbaum Proc. Natl. Acad. Sci. U.S.A. 106 2009 13679
    • (2009) Proc. Natl. Acad. Sci. U.S.A. , vol.106 , pp. 13679
    • Maayan, G.1    Ward, M.D.2    Kirshenbaum, K.3
  • 13
    • 0000477891 scopus 로고
    • For selected examples of the cyanosilylation of aldehydes with a variety of catalysts, see
    • For selected examples of the cyanosilylation of aldehydes with a variety of catalysts, see: D.A. Evans, and L.K. Truesdale Tetrahedron Lett. 14 1973 4929
    • (1973) Tetrahedron Lett. , vol.14 , pp. 4929
    • Evans, D.A.1    Truesdale, L.K.2
  • 31
    • 0000110479 scopus 로고
    • For selected examples of the enantioselective cyanosilylation of aldehydes, see
    • For selected examples of the enantioselective cyanosilylation of aldehydes, see: S. Kobayashi, Y. Tsuchiya, and T. Mukaiyama Chem. Lett. 20 1991 541
    • (1991) Chem. Lett. , vol.20 , pp. 541
    • Kobayashi, S.1    Tsuchiya, Y.2    Mukaiyama, T.3
  • 45
    • 0001661818 scopus 로고
    • For examples of the cyanosilylation with amine catalysts, see
    • For examples of the cyanosilylation with amine catalysts, see: S. Kobayashi, Y. Tsuchiya, and T. Mukaiyama Chem. Lett. 20 1991 537
    • (1991) Chem. Lett. , vol.20 , pp. 537
    • Kobayashi, S.1    Tsuchiya, Y.2    Mukaiyama, T.3
  • 48
    • 24644518441 scopus 로고    scopus 로고
    • For examples of the cyanosilylation with amino acid salts, see
    • For examples of the cyanosilylation with amino acid salts, see: X. Liu, B. Qin, X. Zhou, B. He, and X. Feng J. Am. Chem. Soc. 127 2005 12224
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 12224
    • Liu, X.1    Qin, B.2    Zhou, X.3    He, B.4    Feng, X.5
  • 51
    • 12344335090 scopus 로고    scopus 로고
    • For selected examples of using supported catalysts in the cyanosilylation of aldehydes, see
    • For selected examples of using supported catalysts in the cyanosilylation of aldehydes, see: B. Karimi, and L. Ma'Mani Org. Lett. 6 2004 4813
    • (2004) Org. Lett. , vol.6 , pp. 4813
    • Karimi, B.1    Ma'Mani, L.2
  • 60
    • 0141578843 scopus 로고
    • For examples of the Juliá-Colonna reaction with supported poly(amino acid)s, see
    • For examples of the Juliá-Colonna reaction with supported poly(amino acid)s, see: S. Banfi, S. Colonna, and H. Molinari Tetrahedron 40 1984 5207
    • (1984) Tetrahedron , vol.40 , pp. 5207
    • Banfi, S.1    Colonna, S.2    Molinari, H.3
  • 72
    • 27144559611 scopus 로고    scopus 로고
    • Tenta Gel-supported peptides for organocatalytic reactions have been developed by our group, see
    • Tenta Gel-supported peptides for organocatalytic reactions have been developed by our group, see: K. Akagawa, S. Sakamoto, and K. Kudo Tetrahedron Lett. 46 2005 8185
    • (2005) Tetrahedron Lett. , vol.46 , pp. 8185
    • Akagawa, K.1    Sakamoto, S.2    Kudo, K.3
  • 81
    • 0025232814 scopus 로고
    • n (n = 1-5), were synthesized by the standard method of Fmoc solid-phase peptide synthesis, see
    • n (n = 1-5), were synthesized by the standard method of Fmoc solid-phase peptide synthesis, see: G.B. Fields, and R.L. Noble Int. J. Pept. Protein Res. 35 1990 161
    • (1990) Int. J. Pept. Protein Res. , vol.35 , pp. 161
    • Fields, G.B.1    Noble, R.L.2
  • 82
    • 33748545653 scopus 로고    scopus 로고
    • For reviews of amino acid N-carboxyanhydrides, see
    • For reviews of amino acid N-carboxyanhydrides, see: H.R. Kricheldorf Angew. Chem., Int. Ed. 45 2006 5752
    • (2006) Angew. Chem., Int. Ed. , vol.45 , pp. 5752
    • Kricheldorf, H.R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.