Synthesis of some novel annelated 1,2,3-selena/thiadiazoles and 2h-diazaphospholes
✍ Scribed by Venkatapuram Padmavathi; Dandu Bhaskar Reddy; Tippireddy Venkat Ramana Reddy; Kamireddy Audisesha Reddy
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2003
- Tongue
- English
- Weight
- 50 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
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 characterized by their physical and spectral data.
📜 SIMILAR VOLUMES
## 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.
## Abstract Novel sulfur‐linked bis‐heterocycles, bis‐1,2,3‐selenadiazoles **4**, 1,2,3‐thiadiazoles **5**, and 2__H__‐diazaphospholes **7**, were synthesized from bis(2‐oxo‐2‐phenylethanone)sulfide **2** by adopting a simple and well‐versed methodology. © 2008 Wiley Periodicals, Inc. Heteroatom Ch