Synthesis of NovelC2-Symmetrical Diamino Thioethers Derived from Amino Acids
✍ Scribed by Christoffers, Jens
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 672 KB
- Volume
- 1997
- Category
- Article
- ISSN
- 0947-3440
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✦ Synopsis
Abstract
Chiral β‐amino alcohols 2, available from natural α‐amino acids by reduction, have been converted in a sequence of N‐protection, O‐activation, thioether formation, and deprotection to novel C~2~‐symmetrical β,β′‐diamino thioethers 1, which shall serve as chiral tridentate ligands in late transition metal complexes. Optical purity of compounds 1 was established by amide formation with (+)‐O‐acetylmandelic acid.
📜 SIMILAR VOLUMES
IN connexion with our studies on the antibiotic, Thiostrepton,' we have prepared a number of 2-(a-aminoalkyl)-thiazole-4-carboxylic acids (I, R=H, Me, Et end CHMe2). Since thiazole structures have been advanced for degradation products of other peptide antibiotics, 2,j a brief account of our results
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v