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Volumn 69, Issue 42, 2013, Pages 8885-8898

Trading N and O: Asymmetric syntheses of β-hydroxy-α-amino acids via α-hydroxy-β-amino esters

Author keywords

Hydroxy amino acids; Asymmetric synthesis; Aziridine; Conjugate addition; Lithium amide

Indexed keywords

AZIRIDINE; AZIRIDINE DERIVATIVE; ESTER; HYDROXYL GROUP; ION EXCHANGE RESIN; PHENYLSERINE; THREONINE;

EID: 84883490234     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2013.08.007     Document Type: Article
Times cited : (32)

References (93)
  • 55
    • 2942644316 scopus 로고    scopus 로고
    • We have previously prepared a 5-(tert-butoxycarbonyl)oxazolidin-2-one upon rearrangement of a N-Boc protected β-amino ester by activation of an α-hydroxyl group as the corresponding mesylate; see
    • We have previously prepared a 5-(tert-butoxycarbonyl)oxazolidin-2-one upon rearrangement of a N-Boc protected β-amino ester by activation of an α-hydroxyl group as the corresponding mesylate; see: S.G. Davies, D.G. Hughes, R.L. Nicholson, A.D. Smith, and A.J. Wright Org. Biomol. Chem. 2 2004 1549
    • (2004) Org. Biomol. Chem. , vol.2 , pp. 1549
    • Davies, S.G.1    Hughes, D.G.2    Nicholson, R.L.3    Smith, A.D.4    Wright, A.J.5
  • 69
    • 0031035741 scopus 로고    scopus 로고
    • 3J coupling constants in the order of 8-9 Hz, are diagnostic of their relative configurations; for example, see:, See also Refs. 4b,23b
    • 3J coupling constants in the order of 8-9 Hz, are diagnostic of their relative configurations; for example, see: G. delle Monache, M.C. Di Giovanni, D. Misiti, and G. Zappia Tetrahedron: Asymmetry 8 1997 231 See also Refs. 4b,23b
    • (1997) Tetrahedron: Asymmetry , vol.8 , pp. 231
    • Delle Monache, G.1    Di Giovanni, M.C.2    Misiti, D.3    Zappia, G.4
  • 81
    • 77954103643 scopus 로고    scopus 로고
    • 3-mediated ring-opening hydrofluorination of a range of aryl epoxides, which also proceeded with retention of configuration, see
    • 3-mediated ring-opening hydrofluorination of a range of aryl epoxides, which also proceeded with retention of configuration, see: A.J. Cresswell, S.G. Davies, J.A. Lee, P.M. Roberts, A.J. Russell, J.E. Thomson, and M.J. Tyte Org. Lett. 12 2010 2936
    • (2010) Org. Lett. , vol.12 , pp. 2936
    • Cresswell, A.J.1    Davies, S.G.2    Lee, J.A.3    Roberts, P.M.4    Russell, A.J.5    Thomson, J.E.6    Tyte, M.J.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.