Bicyclic thiohydantoins were synthesized in a stereoselective manner by reacting (2R)/(2S)-diastereoisomer mixtures of 1.3-thiazolidine-2,4-dicarboxylic acids or their dimethyl diesters with PhNCS. 5S-Dimethyl-1 Jthiazolidine-2,4-dicarboxylic acid with PhNCS led to a cyclization involving the C = O
ChemInform Abstract: Diastereo- and Regioisomeric Bicyclic Thiohydantoins from Chiral 1,3-Thiazolidine-2,4-dicarboxylic Acids.
β Scribed by I. MISKOLCZI; A. ZEKANY; F. RANTAL; A. LINDEN; K. E. KOEVER; Z. GYOERGYDEAK
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 32 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Diastereo-and Enantioselective Synthesis of β 2 -1,2,4-Oxadiazolines by 1,3-Dipolar Cycloaddition of Nitrile Oxides with Chiral Hydrazones. -1,3-Dipolar cycloaddition of phenyl nitrile oxide with chiral hydrazones (I) affords β 2 -1,2,4-oxadiazolines (III) with low to excellent diastereoselectiviti
## 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 βFull Textβ option. The original article is trackable v