Please use this identifier to cite or link to this item: http://dspace.iiti.ac.in:8080/jspui/handle/123456789/1144
Title: Synthesis of tubuphenylalanine
Authors: Priyanka
Chelvam, Venkatesh [Supervisor]
Keywords: Chemistry
Issue Date: 29-Jun-2018
Publisher: Discipline of Chemistry, IIT Indore
Series/Report no.: MS78;
Abstract: In this work, we have developed an efficient synthetic route for gram-scale synthesis of N-Boc-tubuphenylalanine benzyl ester (N-Boc-Tup-OBn) and N-Boc-epi-tubuphenylalanine benzyl ester (N-Boc-epi-Tup-OBn). These -aminoacid intermediates are key components for synthesis of anticancer tetrapeptides, tubulysins and can be used to derive novel tubulysin architectures with better therapeutic indices. A regio- and stereoselective hydroboration of (R)-4-methyl-N-(4-methyl-1-phenylpent-4-en-2yl)benzenesulfonamide and subsequent in situ oxidation in alkaline medium was used as the key step to provide corresponding N-tosyl 1,4-amino alcohols, which were effectively transformed into the desired y-aminoacid intermediates in overall excellent yields.
URI: http://dspace.iiti.ac.in:8080/jspui/handle/123456789/1144
Appears in Collections:Discipline of Chemistry

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