Indexed by:
Abstract:
The one-pot synthesis of quinazoline-2,4-diones was developed in the presence of 4-dimethylaminopyridine (DMAP) by metal-free catalysis. The commercially available (Boc)(2)O acted as a key precursor in the construction of the 2-position carbonyl of quinazolinediones. The p-methoxybenzyl (PMB)-activated hetero- cyclization could smoothly proceed at room temperature instead of the microwave condition. This strategy is compatible with a variety of substrates with different functional groups. Furthermore, this protocol was utilized to smoothly prepare Zenarestat with a total yield of 70%.
Keyword:
Reprint Author's Address:
Email:
Source :
ACS OMEGA
ISSN: 2470-1343
Year: 2020
Issue: 16
Volume: 5
Page: 9614-9623
4 . 1 0 0
JCR@2022
Cited Count:
WoS CC Cited Count: 20
SCOPUS Cited Count: 21
ESI Highly Cited Papers on the List: 0 Unfold All
WanFang Cited Count:
Chinese Cited Count:
30 Days PV: 17