Phenacylsulfonylacetic acid methyl ester-synthon for 1,2,3-selena/thiadiazoles and 2H-diazaphospholes
✍ Scribed by Venkatapuram Padmavathi; Konda Mahesh; Pinnu Thriveni; Tippireddy Venkata Ramana Reddy
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2007
- Tongue
- English
- Weight
- 263 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
magnified image
A new class of 1,2,3‐selena/thiadiazoles and 2__H__‐diazaphospholes were synthesized by exploiting α‐ketomethylene group in phenacylsulfonylacetic acid methyl ester.
📜 SIMILAR VOLUMES
## Abstract A number of annelated heterocyclic indene derivatives having 1,2,3‐selena/thiadiazole and 2__H__‐1,2,3‐diazaphosphole rings have been synthesized by exploiting the α‐ketomethylene functionality in some novel 1‐methyl‐piperidin‐4‐ones and 1‐oxo‐tetrahydrothiopyran‐4‐ones and were charact
The carbon and proton spectra of the title compound were completely assigned on the basis of COSY, HETCOR, DEPT and selective single-frequency decoupling experiments. The validity of the proton-proton coupling constants determination was checked by computer simulation.