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Volumn 50, Issue 1, 1994, Pages 265-274

Total Syntheses of Phytosiderophores, 3-Epi-Hydroxymugineic Acid, Distichonic Acid A, and 2′-Hydroxynicotianamine

Author keywords

[No Author keywords available]

Indexed keywords

2' HYDROXYNICOTIANAMINE; 3 EPIHYDROXYMUGINEIC ACID; AMIDE; DISTICHONIC ACID A; MUGINEIC ACID; PHYTOSIDEROPHORE; SIDEROPHORE; UNCLASSIFIED DRUG;

EID: 0028115578     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(01)80749-3     Document Type: Article
Times cited : (48)

References (30)
  • 2
  • 8
  • 9
    • 0025150017 scopus 로고
    • A new stereoselective synthesis of a γ-azetidinylgb-hydroxy-α-amino acid moiety of mugineic acid — a formal synthesis of mugineic acid
    • For the formal syntheses of 1, see
    • (1990) Tetrahedron Letters , vol.31 , pp. 5041
    • Hamada1    Iwai2    Shioiri3
  • 11
    • 1542404690 scopus 로고
    • Tartaric Acid Derived Aziridines as Chiral Precursors of 3-Amino-3-deoxy and 2-Amino-2-deoxy Tetroses: An Efficient Approach Towards Mugineic Acid
    • For the approach toward 1, see
    • (1992) Synlett , pp. 527
    • Carreaux1    Duréault2    Depezay3
  • 16
    • 85046521687 scopus 로고
    • Corrigenda
    • Preliminary communication, Description of the absolute configurations of 2,3-epoxycinnamyl alcohols in the preliminary communication should be revised: (R,R) → (S,S).
    • (1993) Tetrahedron Letters , vol.34 , pp. 2394
    • Matsuura1    Hamada2    Shioiri3
  • 20
    • 84914002455 scopus 로고    scopus 로고
    • Transformation of 10 to 11 could be also achieved by use of NaH in DMF at 0°C.
  • 22
    • 33748638545 scopus 로고
    • Efficient oxidation of phenyl groups to carboxylic acids with ruthenium tetraoxide. A simple synthesis of (R)-.gamma.-caprolactone, the pheromone of Trogoderma granarium
    • (1990) The Journal of Organic Chemistry , vol.55 , pp. 1928
    • Nunez1    Martin2
  • 23
    • 85004388152 scopus 로고
    • New methods and reagents in organic synthesis. 14. A simple efficient preparation of methyl esters with trimethylsilyldiazomethane (TMSCHN2) and its application to gas chromatographic analysis of fatty acids.
    • (1981) CHEMICAL & PHARMACEUTICAL BULLETIN , vol.29 , pp. 1475
    • Hashimoto1    Aoyama2    Shioiri3
  • 26
    • 84914002454 scopus 로고    scopus 로고
    • 4 This might be due to the difference of the reactivity between the imino group (azetidine moiety in the previous paper) and the amino group of 18.
  • 28
    • 84914002453 scopus 로고    scopus 로고
    • 1b
  • 30
    • 84914002452 scopus 로고    scopus 로고
    • Transesterfication from the benzyl ester of 35 to the methyl ester occurred by using MeOH as the solvent instead of i-PrOH.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.