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Thiazolines (/θaɪˈæzoʊliːnz/; or dihydrothiazoles) are a group of isomeric 5-membered heterocyclic compounds containing both sulfur and nitrogen in the ring. Although unsubstituted thiazolines are rarely encountered themselves, their derivatives are more common and some are bioactive. For example, in a common post-translational modification, cysteine…
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thiazolines common cysteine references example standard state isomers synthesis also thiazole 2-thiazoline isomeric sulfur nitrogen derivatives double prepared acid θaɪˈæzoʊliːnz
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Thiazoline | is a | most common.A fourth structure exists in which the N and S atoms are adjacent | 0.90 | text |
| Thiazoline | has application | Many | 0.60 | section |
| Thiazoline | has application | Firefly | 0.60 | section |
| Thiazoline | has application | The | 0.60 | section |
| Thiazoline | has application | Aminothiazoline-4-carboxylic | 0.60 | section |
| Thiazoline | has application | L-cysteine | 0.60 | section |
| Thiazoline | related to Isomers | Three | 0.60 | section |
| Thiazoline | related to Isomers | These | 0.60 | section |
| Thiazoline | related to Isomers | Of | 0.60 | section |
| Thiazoline | related to Synthesis | Thiazolines | 0.60 | section |
| Thiazoline | related to Synthesis | Richard Willstatter | 0.60 | section |
| Thiazoline | related to Synthesis | They | 0.60 | section |
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