EventsThe 4th International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session a. General Organic Synthesis of the event The 4th International Electronic Conference on Synthetic Organic Chemistry
Published date
11 Sep, 2000
Citation
Branko Stanovnik, 3-Dimethylaminopropenoates and Related Compounds in the Synthesis of Heterocyclic Systems and Heterocyclic Amino Acids, in Proceedings of The 4th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2000, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-4-01783
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3-Dimethylaminopropenoates and Related Compounds in the Synthesis of Heterocyclic Systems and Heterocyclic Amino Acids

Branko Stanovnik 1
1. Faculty of Chemistry and Chemical Technology, University of Ljubljana, Askerceva 5, P. O. Box 537, 1000 Ljubljana, Slovenia
Abstract
a -Amino and a -hydroxy acids and their derivatives play an important role in organic synthesis, especially in asymmetric synthesis as chiral synthons, chiral auxiliaries, and resolving agents [1-3]. In the course of our studies of heteroaryl substituted a -amino and a -hydroxy acids and their derivatives we have prepared easily accessible 2-acylamino-3-dimethylaminopropenoates, 2-(O-substituted hydroxy)-3- dimethylaminopropenoates, and 2-ethenylamino-3-dimethylaminopropenoates, masked a -formyl-a -amino- and a - formyl-a -hydroxy acids, and their derivatives. They have turned out to be excellent reagents for the preparaton of a variety of heterocyclic systems with an amino or hydroxy acid structural element incorporated or partially incorporated into the newly formed heterocyclic ring [4]
Keywords
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