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Volumn 22, Issue 6, 1999, Pages 624-628

A formal asymmetric synthesis of mugineic acid: An efficient synthetic route through chiral oxazolidinone

Author keywords

Amino acids; Angiotensin converting enzyme; Formal asymmetric total synthesis; Homoserine; Mugineic acid; Oxazole; Oxazolidinone; Phytosiderophore

Indexed keywords

AMINO ACID; AZETIDINE 2 CARBOXYLIC ACID; DRUG DERIVATIVE; EPOXIDE; HOMOSERINE; MUGINEIC ACID; OXAZOLE DERIVATIVE;

EID: 0033251111     PISSN: 02536269     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02975336     Document Type: Article
Times cited : (7)

References (11)
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  • 3
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  • 4
    • 33845374056 scopus 로고
    • Synthesis of Mugineic through Direct C-Acylation Using Diphenyl Phosphorazidate
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  • 5
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    • Hamada, Y., Iwai, K., and Shioiri, T., A new stereoselective synthesis of a γ-azetidinyl-β-hydroxy-α-amino acid moiety of mugineic acid. A formal synthesis of mugineic acid. Tetrahedron Lett., 31, 5041-5042 (1990).
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  • 6
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    • Synthesis of β-hydroxyhomoserine, constituent of mugineic acid
    • Jung, Y. H., and Won, S. R., Synthesis of β-hydroxyhomoserine, constituent of mugineic acid. Yakhak Hoeji, 37, 437-441 (1993).
    • (1993) Yakhak Hoeji , vol.37 , pp. 437-441
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  • 7
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    • Total synthesis of mugineic acid. Efficient use of the phenyl group as the carboxyl synthon
    • Matsuura, F., Hamada, Y., and Shioiri, T., Total synthesis of mugineic acid. Efficient use of the phenyl group as the carboxyl synthon. Tetrahedron, 49, 8211-8222 (1993).
    • (1993) Tetrahedron , vol.49 , pp. 8211-8222
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  • 8
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    • Directed openings of 2,3-epoxy alcohols via reactions with isocyanates: Synthesis of (+)-erythro-dihydrosphingosine
    • Roush, W. R. and Adam, M. A., Directed openings of 2,3-epoxy alcohols via reactions with isocyanates: Synthesis of (+)-erythro-dihydrosphingosine. J. Org. Chem., 50, 3752-3757 (1985).
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  • 9
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    • A stereochemically general synthesis of 2-deoxyhexoses via the asymmetric allylboration of 2,3-epoxyaldehyde
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.