Synthesis of a new series of 2-(2-oxo-2H-chromen-3-yl)-5H-chromeno[4,3-b]pyridin-5-ones by two facile methods and evaluation of their antimicrobial activity
✍ Scribed by Patel, Apoorva A.; Lad, Hemali B.; Pandya, Kinnar R.; Patel, Chirag V.; Brahmbhatt, Dinkar I.
- Book ID
- 120168440
- Publisher
- Springer-Verlag
- Year
- 2013
- Tongue
- English
- Weight
- 346 KB
- Volume
- 22
- Category
- Article
- ISSN
- 1054-2523
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract magnified image Anhydrous zinc bromide catalysed reactions of arylidine‐3‐acetyl coumarins (**1a‐c**) and 5,6‐benzoanalogs of arylidine 3‐acetyl coumarins (**4a,4b**) with 1,3‐cyclohexanedione gives ‐(4‐aryl‐5‐oxo‐5,6,7,8‐tetrahydro‐4__H__‐chromen‐2yl)‐2__H__‐chromen‐2‐ones (**3a, 3c**
## Abstract Synthesis of 3‐(3‐nitrophenacyl)thiazolidine‐2,4‐dione **2g** and 3‐(substituted phenacyl)‐5‐[3′‐(4__H__‐4‐oxo‐1‐benzopyran‐2‐yl)‐benzylidene]‐2,4‐thiazolidinediones **4a–g** are reported in this paper. These compounds **4a–g** were prepared from 3′‐flavone carboxaldehyde and 3‐substitu