Formation of Aziridine-2-amides through 5-Halo-6-methylperhydropyrimidin-4-ones. A Route to Enantiopure l- and d-Threonine and allo-Threonine
Author:
Affiliation:
1. Dipartimento di Chimica “G. Ciamician” and C.S.F.M., Università di Bologna, Via Selmi, 2-40126 Bologna, Italy
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo971388s
Reference26 articles.
1. (a) Fanta, P. E.Heterocyclic Compounds with Three andFour-membered Rings;Weissemberg, A., Ed.; Wiley-Interscience: New York, 1964; Part 1, p 524.
2. Chiral Aziridines—Their Synthesis and Use in Stereoselective Transformations
3. Highly diastereoselective alkylation of 6-methylperihydropyrimidin-4-ones directed towards the synthesis of α-substituted β-amino acids
4. Synthesis and stereochemical behaviour of 8-alkyl-3-(1-phenylethyl)-7-oxa-1,3-diazabicyclo-[3.2.1]-octane-4,6-diones directed towards the synthesis of α-substituted β-amino acids
5. Highly Diastereoselective Alkylation of Perhydropyrimidin-4-ones Directed toward the Synthesis of .alpha.-Substituted .beta.-Amino Acids. 2.
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3. Alkylation and Related Reactions IV;Key Chiral Auxiliary Applications;2014
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