Efficient One-Pot Synthesis of 3-Amino-7-azaindoles Under Microwave Irradiation
✍ Scribed by Yang, Hai-Kui; You, Wen-Wei; Yan, Guang-Hua; Jiang, Zhi-Hong; Zhao, Pei-Liang; Zhou, Zhong-Zhen
- Book ID
- 121454022
- Publisher
- Taylor and Francis Group
- Year
- 2014
- Tongue
- English
- Weight
- 227 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0039-7911
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract magnified image A series of 3,3‐dimethyl‐9‐substituted‐1,2,3,4,9,10‐hexahydrobenzo[__c__] acridine‐1‐ones and 3,3‐dimethyl‐9‐substituted‐1,2,3,4,9,10‐hexahydrobenzo[__a__] acridine‐1‐ones were synthesized by the reaction of an aldehyde, α‐naphthylamine or β‐naphthylamine and dimedone u
A series of pyrimidoquinoline derivatives were synthesized through one-pot condensation of 2,6diaminopyrimidin-4-one, aldehyde and cyclic a 1,3-dicarbonyl compound in glycol under microwave irradiation without catalyst. The protocol in the absence of catalyst has the advantage of good yield (87-95%)