cas 34441-14-0, 1-Azetidinebutanoic acid, alpha-((3-amino-3-carboxypropyl)amino)-2-car boxy-, (2S-(1(alphaR*(R*)),2R*))- | Articles data ｜lookchem

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34441-14-0

Articles about 34441-14-0Total 7 be found

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A novel synthetic approach towards phytosiderophores: Expeditious synthesis of nicotianamine and 2'-deoxymugineic acid
A short and a novel approach for synthesis of nicotianamine, 2'- deoxymugineic acid and related phytosiderophores has been achieved through peptide intermediates. Selective amide reduction in the presence of ester functionalities by conversion to thioamid
Klair, Sukhbinder S.,Mohan, Hindupur R.,Kitahara, Takeshi
p. 89 - 92
(2007/10/03)

A new efficient synthesis of nicotianamine and 2′-deoxymugineic acid
Nicotianamine and 2′-deoxymugineic acid, phytosiderophores, have been efficiently synthesized, which will be suitable for large scale production of these plant physiologically important compounds. The synthetic method for 2′,3″-dideoxy-3″-oxomugineic acid was also investigated.
Shioiri, Takayuki,Irako, Naoko,Sakakibara, Sachiko,Matsuura, Fumiyoshi,Hamada, Yasumasa
p. 519 - 530
(2007/10/03)

Total Synthesis of 2'-Deoxymugineic Acid and Nicotianamine
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.
Matsuura, Fumiyoshi,Hamada, Yasumasa,Shioiri, Takayuki
p. 9457 - 9470
(2007/10/02)

Optimierung der Synthese von Nicotianamin aus L-Azetidin-2-carbonsaeure
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Prochazka, Zelimir,Rudolph, Armin
p. 336
(2007/10/02)

The "Normalizing Factor" for the Tomato Mutant chloronerva. XXV. Synthesis of 2-Epinicotianamine and Nicotianamine
2-Epinicotianamine (6) was synthesized by stepwise reductive alkylation of ethyl (R)-2-azetidinecarboxylate (2) with ethyl (S)-4-oxo-2-(trifluoroacetylamino)butanoate (3); nicotianamine (8) was prepared in an analogous manner from (2S,αS)-α-amino-2-carboxy-1-azetidinebutanoic acid (7). 2-Epinicotianamine and nicotianamine showed the same biological activity with regard to the phenotypical normalization of the tomato mutant chloronerva.
Ripperger, H.,Schreiber, K.
p. 231 - 234
(2007/10/02)

Eine verbesserte Synthese von Nicotianamin
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Faust, J.,Schreiber, K.,Ripperger, H.
p. 305
(2007/10/02)

SYNTHESIS OF NICOTIANAMINE AND A RELATED COMPOUND, DERIVATIVES OF AZETIDINE-2-CARBOXYLIC ACID
The synthesis of nicotianamine (1) and a related compound (2) - amino acid derivatives having the azetidine ring - was achieved by reductive coupling of L-aspartic-β-semialdehyde derivatives with L-azetidine-2-carboxylic acid methyl ester.
Fushiya, Shinji,Nakatsuyama, Shuichi,Sato, Yoshikazu,Nozoe, Shigeo
p. 819 - 822
(2007/10/02)

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78146-56-2
di-(4-bromobenzoyl) trimethyl ester of nicotianamine

Chemical Properties

Melting Point: >220°C dec.
Boiling Point: 633.3°Cat760mmHg
Flash Point:336.8°C
Density: 1.421g/cm³
Storage Temp.:Hygroscopic, -20?C Freezer, Under Inert Atmosphere
Vapor Pressure: 0mmHg at 25°C
PKA: 2.05±0.10(Predicted)
PSA: 153.19000
LogP: -0.59070

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