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- One-step metal-free construction of fluorescent 5-aryl-2,3-dicyanofurans from simple aryl ketones with DDQ. Jiang-Sheng Li, Fei-Fei Cai, Zhi-Wei Li, Wei-Dong Liu, Jim Simpson, Yuan Xue, Huai-Lin Pang, Peng-Mian Huang, Zhong Cao, Dao-Lin Li
, RSC Adv.
, 2014
, 4
, 474
- Low-dose paeonol derivatives alleviate lipid accumulation. Kuan-Chuan Pao, Jin-Feng Zhao, Tzong-Shyuan Lee, Ying-Pei Huang, Chien-Chung Han, Lin-Chiang Sherlock Huang, Kou-Hung Wu, Ming-Hua Hsu
, RSC Adv.
, 2015
, 5
, 5652
- Eutectic-based liposome as a potential delivery system of paeonol. Jieyu Wu, Suqin Yang, Tianxiang Yin, Xiaoyong Wang
, RSC Adv.
, 2021
, 11
, 39343
- Formylation and bromination ortho to the hydroxy-group of 2-carbonylsubstituted phenols in the presence of titanium(VI)chloride. T. M. Cresp, M. V. Sargent, J. A. Elix, D. P. H. Murphy
, J. Chem. Soc., Perkin Trans. 1
, 1973
, 340
- Divergent synthesis of biflavonoids yields novel inhibitors of the aggregation of amyloid β (1–42). Tze Han Sum, Tze Jing Sum, Súil Collins, Warren R. J. D. Galloway, David G. Twigg, Florian Hollfelder, David R. Spring
, Org. Biomol. Chem.
, 2017
, 15
, 4554
- 219. Derivatives of hydroxyquinol. Part I. Compounds related to 3 : 4 : 6-trimethoxy-2-propenylacetophenone. F. M. Dean, D. R. Randell, Graham Winfield
, J. Chem. Soc.
, 1959
, 1071
- 64. Studies in the pyrone series. Part III. The influence of the phenyl group in the kostanecki reaction. I. M. Heilbron, D. H. Hey, B. Lythgoe
, J. Chem. Soc.
, 1936
, 295
- 345. Studies in the pyrone series. Part II. Chromones and coumarins derived from 2-hydroxy-4-methoxy-aceto- and -propio-phenones. I. M. Heilbron, D. H. Hey, B. Lythgoe
, J. Chem. Soc.
, 1934
, 1581
- A simple coumarin as a turn-on fluorescence sensor for Al(iii) ions. Tianrong Li, Ran Fang, Baodui Wang, Yongliang Shao, Jian Liu, Shouting Zhang, Zhengyin Yang
, Dalton Trans.
, 2014
, 43
, 2741
- Red fluorescence from tautomers of 2′-hydroxychalcones induced by intramolecular hydrogen atom transfer. Takeshi Teshima, Madoka Takeishi, Tatsuo Arai
, New J. Chem.
, 2009
, 33
, 1393