## Abstract The 6‐chloro‐2‐cyclohexenones **3, 6** and **11**, and the 5‐chloro‐2‐cyclopentenone **15** were newly synthesized. The results obtained with compounds **3** and **15** in photocycloadditions to olefins show that the oxetane __vs.__ cyclobutane product ratio is reduced by the substituti
Photochemistry of 4-Thia-2-cycloalkenones. Part 2
✍ Scribed by Elke Anklam; Sabine Lau; Paul Margaretha
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- German
- Weight
- 205 KB
- Volume
- 68
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Methyl 2‐allyl‐3‐oxo‐2,3‐dihydrothiophene‐2‐carboxylate (2) photocyclizes selectively to methyl 2‐oxo‐7‐thiatricyclo[3.2.1.0^3,6^]octane‐1‐carboxylate (4). In contrast, 4‐thia‐2‐cyclohexenone 3, on irradiation, affords only low yields of dimers, cycloadducts (2‐methylpropene) or RH reduction products (i‐ProH).
📜 SIMILAR VOLUMES
## 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
## Abstract Irradiation (λ > 370 nm) of 4,4‐dimethoxy‐2,5‐cyclohexadienone (**1 a**) in benzene affords mainly the ketene acetal **4 a**, which then undergoes further rearrangement. The carbomethoxycyclopentenones **6** and **7** were isolated in modest yields (10–15°). It is conceivable that the l