𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Photochemical cycloadditions of thioparabanates to olefins

✍ Scribed by Hans Gotthardt; Sonja Nieberl


Publisher
Elsevier Science
Year
1974
Tongue
French
Weight
171 KB
Volume
15
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis


Diarylthioketones 1,2 , thiophosgene3, and thione carbonates 4 react with substituted alkenes under photochemical conditions to give thietanes and in some cases, 1,4-dithianes. It is known that thioparabanates, A, undergo photoreduction in ethanolic solution5. However, the formation of a small amount (3%) of a thietane derivative has also been observed in the reaction of 18 with 2-5 methyl-2-butene


πŸ“œ SIMILAR VOLUMES


Photochemical Olefin-Aziridine Cycloaddi
✍ Dr. Michael Klaus; Prof. Dr. Horst Prinzbach πŸ“‚ Article πŸ“… 1971 πŸ› John Wiley and Sons 🌐 English βš– 196 KB
1,3-Dipolar Cycloadditions to Strained O
✍ Konrad B. Becker; Martin K. Hohermuth πŸ“‚ Article πŸ“… 1979 πŸ› John Wiley and Sons 🌐 German βš– 764 KB

## Abstract The __Bredt__ olefins bicyclo [3.3.1]non‐1‐ene **(2)**, bicyclo [4.2.1]non‐1 (8)‐ene **(3)**, and bicyclo [4.2.1]non‐1 (2)‐ene **(4)** react rapidly with 1,3‐dipoles such as diazomethane, phenyl azide, and mesitonitrile oxide to yield mixtures of two regioisomeric cycloadducts **10, 11*

Photochemical cycloaddition of cycloocty
✍ R.D. Miller; V.Y. Abraitys πŸ“‚ Article πŸ“… 1971 πŸ› Elsevier Science 🌐 French βš– 208 KB

The photochemical cycloaddition of acetylene to benzene and its simple derivatives leading ultimately to cyclooctatetraenes has enjoyed rather limited applicability. Previously, successful examples were confined to electron deficient acetylenes or activated aromatic systems.' Very recently, Bryce-