Tetrahedron p. 9457 - 9470 (1994)
Update date:2022-08-04
Topics: Oxidation Solid-phase synthesis Column chromatography Yield Stereochemistry Reduction Enantiomeric excess (ee) Total synthesis Mass spectrometry (MS) Enantioselective synthesis High-performance liquid chromatography (HPLC) Deprotection Protecting group Nuclear Magnetic Resonance (NMR) Chelation Retrosynthetic analysis Chiral Auxiliary Peptide Coupling
Matsuura, Fumiyoshi
Hamada, Yasumasa
Shioiri, Takayuki
Steroselective total synthesis of the unique phytosiderophores, 2'-deoxymugineic acid (4) and nicotianamine (5), has been achieved from the β-tyrosine derivative 21 using its aryl groups as the carboxyl synthon.
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Doi:10.1039/d0cc02703k
(2020)Doi:10.1016/j.bmcl.2014.03.053
(2014)Doi:10.1021/ja502275w
(2014)Doi:10.1039/DT9940003039
(1994)Doi:10.1016/j.molcata.2014.02.025
(2014)Doi:10.1246/bcsj.20130267
(2014)
