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Volumn 9, Issue 13, 1998, Pages 2223-2227

Asymmetric synthesis of substituted 1-aminocyclopropane-1-carboxylic acids from a new chiral glycine equivalent with 3,6-dihydro-2H-1,4-oxazin-2- one structure

Author keywords

[No Author keywords available]

Indexed keywords

1 AMINOCYCLOPROPANECARBOXYLIC ACID; GLYCINE DERIVATIVE; OXAZINE DERIVATIVE;

EID: 0032479507     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(98)00244-4     Document Type: Article
Times cited : (25)

References (33)
  • 1
    • 0025074114 scopus 로고
    • For recent reviews see for instance: (a)
    • For recent reviews see for instance: (a) Stammer, C. H.; Tetrahedron 1990, 46, 2231-2254.
    • (1990) Tetrahedron , vol.46 , pp. 2231-2254
    • Stammer, C.H.1
  • 8
    • 0029908901 scopus 로고    scopus 로고
    • 2c ACCs also have important applications in the design and synthesis of peptidomimetics. See, for instance
    • 2c ACCs also have important applications in the design and synthesis of peptidomimetics. See, for instance: Burgess, K.; Ke, C.-Y. J. Org. Chem. 1996, 61, 8627-8631.
    • (1996) J. Org. Chem. , vol.61 , pp. 8627-8631
    • Burgess, K.1    Ke, C.-Y.2
  • 14
    • 0023872535 scopus 로고
    • DDAA derivatives represent an important type of compound as key intermediates in amino acid and peptide synthesis and as constituents of naturally occurring peptides with potent antimicrobial and phytotoxic activities. For reviews see: (a)
    • DDAA derivatives represent an important type of compound as key intermediates in amino acid and peptide synthesis and as constituents of naturally occurring peptides with potent antimicrobial and phytotoxic activities. For reviews see: (a) Schmidt, U.; Lieberknecht, A.; Wild, J. Synthesis 1988, 159-172.
    • (1988) Synthesis , pp. 159-172
    • Schmidt, U.1    Lieberknecht, A.2    Wild, J.3
  • 26
    • 0010711247 scopus 로고
    • 546 +20 (c, 2.2; 95% EtOH) The preparation of 12 following this literature procedure afforded very low yields
    • 546 +20 (c, 2.2; 95% EtOH): Maigrot, N.; Mazaleyrat, J.-P.; Welvart, Z. J. Org. Chem. 1985, 50, 3916-3918. The preparation of 12 following this literature procedure afforded very low yields.
    • (1985) J. Org. Chem. , vol.50 , pp. 3916-3918
    • Maigrot, N.1    Mazaleyrat, J.-P.2    Welvart, Z.3
  • 27
    • 0025036824 scopus 로고
    • This acid is commercially available (Aldrich) or can be prepared by diazotization of L-valine
    • This acid is commercially available (Aldrich) or can be prepared by diazotization of L-valine: Li, W.-R.; Ewing, W. R.; Harris, B. D.; Jouillé, M. M. J. Am. Chem. Soc. 1990, 112, 7659-7672.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 7659-7672
    • Li, W.-R.1    Ewing, W.R.2    Harris, B.D.3    Jouillé, M.M.4
  • 29
    • 0344046144 scopus 로고    scopus 로고
    • note
    • -1. Full structural details have been deposited with the Cambridge Crystallographic Data Centre.
  • 30
    • 33947485009 scopus 로고
    • For a recent review on asymmetric ylide reactions see
    • Corey, E. J.; Chaykovsky, M. J. Am. Chem. Soc. 1965, 87, 1353-1364. For a recent review on asymmetric ylide reactions see: Li, A.-H.; Dai, L.-X.; Aggarzwal, V. K. Chem. Rev. 1997, 97, 2341-2372.
    • (1965) J. Am. Chem. Soc. , vol.87 , pp. 1353-1364
    • Corey, E.J.1    Chaykovsky, M.2
  • 31
    • 0001485086 scopus 로고    scopus 로고
    • Corey, E. J.; Chaykovsky, M. J. Am. Chem. Soc. 1965, 87, 1353-1364. For a recent review on asymmetric ylide reactions see: Li, A.-H.; Dai, L.-X.; Aggarzwal, V. K. Chem. Rev. 1997, 97, 2341-2372.
    • (1997) Chem. Rev. , vol.97 , pp. 2341-2372
    • Li, A.-H.1    Dai, L.-X.2    Aggarzwal, V.K.3
  • 33
    • 0344046142 scopus 로고    scopus 로고
    • note
    • 2O).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.