EventsThe 11th International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session a. General Organic Synthesis of the event The 11th International Electronic Conference on Synthetic Organic Chemistry
Published date
30 Nov, 2007
Citation
Jana Raschmanova, Miroslava Martinkova, Jozef Gonda, Stereoselective synthesis of the advanced precursor of (+)-myriocin, in Proceedings of The 11th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2007, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-11-01307
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Stereoselective synthesis of the advanced precursor of (+)-myriocin

Jana Raschmanova 1
Miroslava Martinkova 1
Jozef Gonda 1
1. P J. Safarik University in Kosice, Faculty of Science, Institute of Chemistry, Debartment of Organic Chemistry, Moyzesova 11, Kosice, Slovak Republic
Abstract
A stereoselective approach toward 2-amino-1,3-propanediol 13 is described. This compound represents the key intermediate in the total stereoselective synthesis of (+)-myriocin 1, an inhibitor of serine palmitoyltransferase (SPT). Moreover, synthon 13 can be used for synthesis of mycriocin analogues. 2-amino-1,3-propanediol moiety is necessary for their biological activity.
Keywords
n/a
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