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Volumn 56, Issue 16, 2000, Pages 2413-2420

Reactions of alkyl radicals with oxime ether: One-pot synthesis of α- amino acids

Author keywords

amino acids; Atom transfer; One pot; Oxime ether; Radical addition

Indexed keywords

ALKYL GROUP; ALPHA AMINO ACID; ETHER; OXIME; RADICAL;

EID: 0034646774     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(00)00119-8     Document Type: Article
Times cited : (57)

References (50)
  • 2
    • 0342975496 scopus 로고    scopus 로고
    • (b) whole issue of No. 2
    • (b) Chem. Rev. 1997, 97, whole issue of No. 2, pp 347-510.
    • (1997) , vol.97 , pp. 347-510
    • Chem., Rev.1
  • 4
    • 0038106171 scopus 로고    scopus 로고
    • For reviews, see: (a)
    • For reviews, see: (a) Bloch, R. Chem. Rev. 1998, 98, 1407.
    • (1998) Chem. Rev. , vol.98 , pp. 1407
    • Bloch, R.1
  • 7
    • 0001271879 scopus 로고    scopus 로고
    • (d) Helmchen, G., Hoffmann, R. W., Mulzer, J., Schaumann, E., Eds.; Thieme: New York
    • (d) Risch, N.; Arend, N. In Stereoselective Synthesis; Helmchen, G., Hoffmann, R. W., Mulzer, J., Schaumann, E., Eds.; Thieme: New York, 1996; Vol. 3; pp 1833-2009.
    • (1996) In Stereoselective Synthesis , vol.3 , pp. 1833-2009
    • Risch, N.1    Arend, N.2
  • 8
  • 9
    • 0032843689 scopus 로고    scopus 로고
    • For selected recent examples, see: (a)
    • For selected recent examples, see: (a) Akiyama, T.; Takaya, J.; Kagoshima, H. Synlett 1999, 1426.
    • (1999) Synlett , pp. 1426
    • Akiyama, T.1    Takaya, J.2    Kagoshima, H.3
  • 14
    • 0032837567 scopus 로고    scopus 로고
    • For reviews, see: (a)
    • For reviews, see: (a) Naito, T. Heterocycles 1999, 50, 505.
    • (1999) Heterocycles , vol.50 , pp. 505
    • Naito, T.1
  • 15
    • 0030666083 scopus 로고    scopus 로고
    • (b)
    • (b) Fallis, A. G.; Brinza, I. M. Tetrahedron 1997, 53, 17543. Oxime ethers are well known to be excellent radical acceptors.
    • (1997) Tetrahedron , vol.53 , pp. 17543
    • Fallis, A.G.1    Brinza, I.M.2
  • 16
    • 0033515460 scopus 로고    scopus 로고
    • Oxime ethers are well known to be excellent radical acceptors. See: (c)
    • See: (c) Miyabe, H.; Fujishima, Y.; Naito, T. J. Org. Chem. 1999, 64, 2174.
    • (1999) J. Org. Chem. , vol.64 , pp. 2174
    • Miyabe, H.1    Fujishima, Y.2    Naito, T.3
  • 30
    • 0033543464 scopus 로고    scopus 로고
    • Alkylative amination of aldehydes based on the radical reaction of oxime ethers, see:
    • Alkylative amination of aldehydes based on the radical reaction of oxime ethers, see: Miyabe, H.; Yamakawa, K.; Yoshioka, N.; Naito, T. Tetrahedron 1999, 55, 11209.
    • (1999) Tetrahedron , vol.55 , pp. 11209
    • Miyabe, H.1    Yamakawa, K.2    Yoshioka, N.3    Naito, T.4
  • 37
    • 0001342149 scopus 로고    scopus 로고
    • For related examples, high 1,3-stereoinduction in radical additions to cyclic imines has recently been reported. See: (c)
    • For related examples, high 1,3-stereoinduction in radical additions to cyclic imines has recently been reported. See: (c) Bertrand, M. P.; Feray, L.; Nouguier, R.; Stella, L. Synlett 1998, 780.
    • (1998) Synlett , pp. 780
    • Bertrand, M.P.1    Feray, L.2    Nouguier, R.3    Stella, L.4
  • 40
    • 0032542749 scopus 로고    scopus 로고
    • For some examples of the synthesis of α-amino acids using glyoxylic imines, see: (a)
    • For some examples of the synthesis of α-amino acids using glyoxylic imines, see: (a) Hagiwara, E.; Fujii, A.; Sodeoka, M. J. Am. Chem. Soc. 1998, 120, 2474.
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 2474
    • Hagiwara, E.1    Fujii, A.2    Sodeoka, M.3
  • 44
    • 0030923305 scopus 로고    scopus 로고
    • V-70 (2,2′-azobis-(2,4-dimethyl-4-methoxyvaleronitrile)) works well as a radical initiator at room temperature. See: (a)
    • V-70 (2,2′-azobis-(2,4-dimethyl-4-methoxyvaleronitrile)) works well as a radical initiator at room temperature. See: (a) Kita, Y.; Sato, A.; Yamaguchi, T.; Oka, M.; Gotanda, K.; Matsugi, M. Tetrahedron Lett. , 38, 3549.
    • Tetrahedron Lett. , vol.38 , pp. 3549
    • Kita, Y.1    Sato, A.2    Yamaguchi, T.3    Oka, M.4    Gotanda, K.5    Matsugi, M.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.