105879-55-8Relevant academic research and scientific papers
A Synthesis of A γ-Azetidinyl-β-hydroxy-α-amino Acid Derivative, A Key Intermediate for the Synthesis of Mugineic Acid
Matsuura, Fumiyoshi,Hamada, Yasumasa,Shioiri, Takayuki
, p. 1069 - 1074 (2007/10/02)
The γ-azetidinyl-β-hydroxy-α-amino acid derivative 2, a key intermediate for the total synthesis of mugineic acid (1), was stereoselectively prepared from readily available (2R,3R)-epoxysuccinic acid (3).
A NEW STEREOSELECTIVE SYNTHESIS OF A γ-AZETIDINYL-β-HYDROXY-α-AMINO ACID MOIETY OF MUGINEIC ACID - A FORMAL SYNTHESIS OF MUGINEIC ACID
Hamada, Yasumasa,Iwai, Kiyotaka,Shioiri, Takayuki
, p. 5041 - 5042 (2007/10/02)
A γ-azetidinyl-β-hydroxy-α-amino acid moiety of mugineic acid (1) was stereoselectively prepared as its protected form 2 from (R)-glyceric acid derivative 3, providing an alternative synthesis of mugineic acid (1).
Synthesis of Mugineic Acid through Direct C-Acylation Using Diphenyl Phosphorazidate
Hamada, Yasumasa,Shioiri, Takayuki
, p. 5489 - 5490 (2007/10/02)
The first synthesis of mugineic acid, a typical phytosiderophore from roots of barley, has been achieved through direct C-acylation using diphenyl phosphorazidate (DPPA).
