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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