A new approach to the synthesis of enantiomerically pure 2,3-diaminoacids through chiral imidazolidin-2-ones
- 1 January 1991
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 47 (12-13) , 2263-2272
- https://doi.org/10.1016/s0040-4020(01)96136-8
Abstract
No abstract availableThis publication has 20 references indexed in Scilit:
- Stereoselective synthesis of 2,3-diamino acids. 2,3-Diamino-4-phenylbutanoic acidThe Journal of Organic Chemistry, 1990
- Synthesis of (R)-N-Tosylemeriamine via ChiralN-Tosylimidazolidin-2-onesSynlett, 1990
- Convenient synthesis of vicinal diaminesThe Journal of Organic Chemistry, 1989
- Stereoselective intramolecular haloamidation of N-protected 3-hydroxy-4-pentenylamines and 4-hydroxy-5-hexenylaminesThe Journal of Organic Chemistry, 1988
- Urea as the most reactive and versatile nitrogen nucleophile for the palladium(2+)-catalyzed cyclization of unsaturated aminesJournal of the American Chemical Society, 1988
- Synthesis of Aminoalcohols via Perihydro-1,3-oxazin-2-ones and Absolute Configuration Assignment through MM2 CalculationsChemistry Letters, 1988
- Tissue distribution properties of technetium-99m-diamide-dimercaptide complexes and potential use as renal radiopharmaceuticalsJournal of Medicinal Chemistry, 1986
- Association phenomena. 7. Mixed chelate and comicellar catalysis of acetyl phosphate olysis reactionsJournal of the American Chemical Society, 1985
- Stereocontrolled synthesis of (+)-negamycin from an acyclic homoallylamine by 1,3-asymmetric inductionJournal of the American Chemical Society, 1982
- Bledta II: Synthesis of a new tumor‐visualizing derivative of CO(III)‐bleomycinJournal of Labelled Compounds and Radiopharmaceuticals, 1981