## Abstract For Abstract see ChemInform Abstract in Full Text.
Synthesis and reactivity of some thiochroman-3,4-diones.
✍ Scribed by Christopher D Gabbutt; John D Hepworth; B.Mark Heron
- Book ID
- 104203202
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- French
- Weight
- 938 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
✦ Synopsis
AbSrrac~ Tbiochmman -3.4-diones. which result from the rextion of thiociuoman-+ooes with isoamyl nitrite, form fused heterocycles on reaction with 1.2diiines and with p-anisaldehyde and ammonium acetate. Cyclopenta-[cl[llaenzothiopyran-2-one. formed on reacdon with dibenzyl ketone, yields a dibenzo[&fJthiopyran after cycloaddition of DMAD. Wii methyl magaesimn iodide, a mixture of thbchnwan-3-and 4-ols ia formed which was separated only after the selective dehydration of the 4-01. The resulting 4-methylene derivative was isolated as the hetero Diels-Alder s*linkedadducr C. D. GABBUTT et al.
📜 SIMILAR VOLUMES
## Abstract An efficient synthesis of 3‐bromoacetyl‐4‐hydroxy‐6‐methyl‐2__H__‐pyran‐2‐one by bromination of dehydroacetic acid in glacial acetic acid is described. Novel 4‐hydroxy‐6‐methyl‐3‐(2‐substituted‐thiazol‐4‐yl)‐2__H__‐pyran‐2‐ones have been prepared from the reaction of 3‐bromoacetyl‐4‐hyd