89965-55-9Relevant academic research and scientific papers
Total Synthesis of the Proposed Structure of Mycobactin J
Ghosh, Chiranjit,Pal, Sujit,Patel, Akanksha,Kapur, Manmohan
supporting information, p. 6511 - 6515 (2018/10/20)
The total synthesis of the proposed structure of mycobactin J (MJ), a metabolite of Mycobacterium tuberculosis, is presented. The highlights of the synthesis include a careful control of the Z-stereochemistry of the unsaturated long chain fatty acid, a biomimetic construction of the oxazoline building block and the carriage of an unprotected phenol throughout the synthesis.
Dehydrative cyclization of serine, threonine, and cysteine residues catalyzed by molybdenum(VI) oxo compounds
Sakakura, Akira,Kondo, Rei,Umemura, Shuhei,Ishihara, Kazuaki
body text, p. 2102 - 2109 (2009/07/11)
Commercially available molybdenum(VI) oxides such as (NH4)2MoO4, (NH4)6Mo7O24·4H2O, MoO2(acac)2, and MoO2(TMHD)2 are highly
Dehydrative cyclization catalyzed by the combination of molybdenum(VI) oxides and benzoic acids: First synthesis of the antitumour substance BE-70016
Sakakura, Akira,Umemura, Shuhei,Kondo, Rei,Ishihara, Kazuaki
, p. 551 - 555 (2008/02/08)
The dehydrative cyclization of N-(o-hydroxybenzoyl)threonine derivative la is efficiently promoted by the combined use of molybdenum(VI) oxides and benzoic acids bearing electron-with-drawing substituents. In the presence of ammonium molybdate [(NH4
Total Synthesis of Parabactin, a Spermidine Siderophore
Nagao, Yoshimitsu,Miyasaka, Tadayo,Hagiwara, Yuichi,Fujita, Eiichi
, p. 183 - 187 (2007/10/02)
The stereoselective total synthesis of parabactin (1) has been efficiently carried out using substituted 1,3-thiazolidine-2-thione as a leaving group.
