The reaction of singlet oxygen with 4,5,6,7-tetrahydro-2-methylbenzothiazole
✍ Scribed by Harry H. Wasserman; George R. Lenz
- Publisher
- Elsevier Science
- Year
- 1974
- Tongue
- French
- Weight
- 182 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
Per-on
Preaa.
📜 SIMILAR VOLUMES
## Abstract __N__‐(2‐Amino‐5,6,7,8‐tetrahydro‐6‐quinazolinyl)acetamide (**9**) and __N__‐(2,4‐diamino‐5,6,7,8‐tetrahydro‐6‐quinazolinyl)acetamide (**6**) were synthesized from __N__‐(4‐oxocyclohexyl)acetamide (**5**) as novel peptidomimetic building blocks. With similar purpose, __N__‐(6‐oxo‐5,6,7,
## Abstract The reaction of singlet oxygen with 2‐phenylnorbornene (**1**) in aprotic solvents gives 3‐formylcyclopentyl phenyl ketone (**2**) (10%) and uncharacterized polymer (90%). When methanol is used as solvent, __endo__‐2‐phenyl‐__exo__‐2‐methoxy‐__exo__‐3‐hydroperoxynorbornane (**4**) and _
The reaction of singlet oxygen with 2-cyclopenten-l-one derivatives is regioselective. Reactivity toward singlet oxygen is not solely determined by the conformation of the carbonyl group relative to the olefinic double bond, since even some s-tran.s derivatives are reasonably reactive.