Efficient synthesis of mugineic acid, a typical phytosiderophore, utilizing the phenyl group as the carboxyl synthon

Tetrahedron Letters

Volumn 33, Issue 51, 1992, Pages 7917-7920

  Matsuura, Fumiyoshi ^a   Hamada, Yasumasa ^a   Shioiri, Takayuki ^a  

^a NAGOYA CITY UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

MUGINEIC ACID; SIDEROPHORE; UNCLASSIFIED DRUG;

ARTICLE; PRIORITY JOURNAL; REACTION ANALYSIS; STEREOCHEMISTRY; SYNTHESIS;

HORDEUM VULGARE SUBSP. VULGARE;

EID: 0027050861     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)74778-2     Document Type: Article

References (23)

1. Structure of Mugineic Acid, a New Amino Acid Possessing an Iron-Chelating Activity from Roots Washings of Water-Cultured Hordeum vulgare L
2. Nicotianamine and Analogous Amino Acids, Endogenous Iron Carriers in Higher Plants
3. Phytosiderophores structures and properties of mugineic acids and their metal complexes
4. A greatly improved procedure for ruthenium tetroxide catalyzed oxidations of organic compounds
5. Efficient oxidation of phenyl groups to carboxylic acids with ruthenium tetraoxide. A simple synthesis of (R)-.gamma.-caprolactone, the pheromone of Trogoderma granarium
6. Esterification and Alkylation Reactions Employing Isoureas
7. Structure and Synthesis of Medicanine, a New Amino Acid from Medicago sativa