Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Yidan Du"'
Autor:
Zhengxi Wang, Jishu Zheng, Decheng Pu, Peiyuan Li, Xiuli Wei, Dongsheng Li, Lihong Gao, Xuliang Zhai, Changhua Zhao, Yidan Du
Publikováno v:
Food Chemistry: X, Vol 24, Iss , Pp 101787- (2024)
To investigate the nutritional quality and flavor characteristics of Micropterus salmoides muscle cultivated in the pond (P), in-pond raceway (IPRS), and industrial aquaponics (ARAS) systems, we comprehensively analyzed texture properties, nutrient c
Externí odkaz:
https://doaj.org/article/e83260c786564dd4b604936c5c02daaf
Publikováno v:
European Journal of Medicinal Chemistry. 74:751-758
A series of phosphorylated flavonoids were synthesized and investigated in vitro as inhibitors of pancreatic cholesterol esterase (CEase) and acetylcholinesterase (AChE). The results showed that most of the synthesized compounds exhibited nanomolar p
Publikováno v:
Heteroatom Chemistry. 22:649-652
In this work, we found that acids (i.e., HCl and NaHSO3) rather than bases could catalyze the cyclization of o-alkynylphenylphosphonic acid monoesters at slow rates and give phosphaisocoumarins in low to medium yields, whereas the cyclization of (o-h
Publikováno v:
The Journal of Organic Chemistry. 73:9012-9015
A series of 4-halophosphaisocoumarins were synthesized via CuX2 (X = Br, Cl) -mediated direct halocyclization of 2-(1-alkynyl)phenylphosphonic acid diesters in dichloroethane with the addition of n-Bu4NX or/and AgI in good to excellent yields. This r
Publikováno v:
ChemInform. 43
The first examples of the synthesis of phosphorus heterocycles via acid- or base-catalyzed intramolecular cyclization reactions of title alkynes are given.
Publikováno v:
ChemInform. 40
A series of 4-halophosphaisocoumarins were synthesized via CuX2 (X = Br, Cl) -mediated direct halocyclization of 2-(1-alkynyl)phenylphosphonic acid diesters in dichloroethane with the addition of n-Bu4NX or/and AgI in good to excellent yields. This r
Publikováno v:
Organic & Biomolecular Chemistry. 9:2530
Five flavones possessing one to four phenolic groups were fully phosphorylated efficiently and the obtained compounds showed excellent pancreatic cholesterol esterase (CEase) inhibitory activities with IC(50) in the nanomolar range, which were much m
Publikováno v:
Journal of Organic Chemistry; 11/21/2008, Vol. 73 Issue 22, p9012-9015, 4p, 3 Diagrams, 3 Charts