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Volumn 3, Issue 20, 2001, Pages 3153-3155

Highly efficient chiral-pool synthesis of (2S,4R)-4-hydroxyornithine

Author keywords

[No Author keywords available]

Indexed keywords

4 HYDROXYORNITHINE; 4-HYDROXYORNITHINE; ASPARTIC ACID; DRUG DERIVATIVE; ORNITHINE;

EID: 0035807577     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol016445p     Document Type: Article
Times cited : (40)

References (29)
  • 12
    • 0042372415 scopus 로고    scopus 로고
    • Dissertation, Universität Heidelberg
    • (a) Mues, H.; Dissertation, Universität Heidelberg, 2000.
    • (2000)
    • Mues, H.1
  • 19
    • 0000851805 scopus 로고
    • Trost, B. M., Ed.; Pergamon: Oxford
    • (b) Rosini, G. In Comprehensive Organic Synthesis; Trost, B. M., Ed.; Pergamon: Oxford, 1991; Vol. 2, p 321.
    • (1991) Comprehensive Organic Synthesis , vol.2 , pp. 321
    • Rosini, G.1
  • 20
    • 0032970032 scopus 로고    scopus 로고
    • For a comprehensive overview on different strategies for the synthesis of aspartaldehyde derivatives, see: Meffre, P. Amino Acids 1999, 76, 251-272.
    • (1999) Amino Acids , vol.76 , pp. 251-272
    • Meffre, P.1
  • 23
    • 0006490803 scopus 로고
    • Earlier studies also indicated that control of stereochemistry is difficult for Henry reactions of nitroalkanes with aldehydes bearing a chiral center in the β-position. See: (a) Moorman, A. R.; Martin, T.; Borchardt, R. T. Carbohydr. Res. 1983, 113, 233-239.
    • (1983) Carbohydr. Res. , vol.113 , pp. 233-239
    • Moorman, A.R.1    Martin, T.2    Borchardt, R.T.3
  • 25
    • 84993904692 scopus 로고
    • Baker, D. C.; Putt, S. R. Synthesis 1978, 478-479. According to the authors, the high preference of C-acylation over O-acylation for the ambidently nucleophilic methanenitronate anion is assigned to the unique reactivity of the acylimidazole which behaves differently from other activated acyl species.
    • (1978) Synthesis , pp. 478-479
    • Baker, D.C.1    Putt, S.R.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.