Can You Really Do Chemisty Experiments About (S)-4-Isopropylthiazolidine-2-thione

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While the job of a research scientist varies, most chemistry careers in research are based in laboratories, where research is conducted by teams following scientific methods and standards. An article , which mentions Application In Synthesis of (S)-4-Isopropylthiazolidine-2-thione, molecular formula is C6H11NS2. The compound – (S)-4-Isopropylthiazolidine-2-thione played an important role in people’s production and life., Application In Synthesis of (S)-4-Isopropylthiazolidine-2-thione

The stereochemical outcome of the Lewis acid-mediated glycolate addition of the titanium enolates from protected N-hydroxyacetyl-4-isopropyl-1,3- thiazolidine-2-thiones to dimethyl and dibenzyl acetals depends on the hydroxyl protecting group. Particularly, the pivaloyl protected glycolate derivative provides the reluctant anti adducts in high yields and diastereomeric ratios, which can be isolated and further converted in enantiomerically pure form to beta-methoxy or beta-benzyloxy alpha-pivaloyloxy carbonyl fragments in a straightforward manner.

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Reference:
Quinuclidine – Wikipedia,
Quinuclidine | C7H717N | ChemSpider