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- A convenient synthesis of new (E)-5-hydroxy-2-styrylchromones by modifications of the Baker–Venkataraman method. Diana C. G. A. Pinto, Artur M. S. Silva, José A. S. Cavaleiro
, New J. Chem.
, 2000
, 24
, 85
- Synergistic or antagonistic antioxidant combinations – a case study exploring flavonoid-nitroxide hybrids. Astrid C. R. Larin, Michael C. Pfrunder, Kathleen M. Mullen, Sandra Wiedbrauk, Nathan R. Boase, Kathryn E. Fairfull-Smith
, Org. Biomol. Chem.
, 2023
, 21
, 1780
- Facile Total Syntheses of Two Novel 4-Alkenyloxy-2,6-dihydroxyacetophenones. Chusheng Huang, Zhe Zhang, Shuhua Li, Yulin Li
, J. Chem. Res. (S)
, 1999
, 148
- Intramolecular catalysis in the detritiation of 2′,6′-dihydroxyacetophenone and 2′-hydroxyacetophenone. Ronald P. Bell, Derek W. Earls
, J. Chem. Soc., Perkin Trans. 2
, 1976
, 45
- Hollow multishelled heterostructures with enhanced performance for laser desorption/ionization mass spectrometry based metabolic diagnosis. Congcong Pei, Rui Su, Songting Lu, Xiaonan Chen, Yajie Ding, Rongxin Li, Weikang Shu, Yu Zeng, Yingying Lin, Liang Xu, Yuqiang Mi, Jingjing Wan
, J. Mater. Chem. B
, 2023
, 11
, 8206
- Quality assessment of Penthorum chinense Pursh through multicomponent qualification and fingerprint, chemometric, and antihepatocarcinoma analyses. Zong-Liang Sun, Yu-Zhen Zhang, Feng Zhang, Jia-Wei Zhang, Guo-Can Zheng, Ling Tan, Chong-Zhi Wang, Lian-Di Zhou, Qi-Hui Zhang, Chun-Su Yuan
, Food Funct.
, 2018
, 9
, 3807
- Unusual base-induced transformations of 2′,6′-dihydroxyacetophenone oxime. P. Crabbé, A. Villarino, J. M. Muchowski
, J. Chem. Soc., Perkin Trans. 1
, 1973
, 2220
- 670. The synthesis of γ-resorcylic acid (2 : 6-dihydroxybenzoic acid). N. J. Cartwright, J. Idris Jones, Diana Marmion
, J. Chem. Soc.
, 1952
, 3499
- Tuning the coordination properties of multi-histidine peptides by using a tripodal scaffold: solution chemical study and catechol oxidase mimicking. Ágnes Dancs, Nóra V. May, Katalin Selmeczi, Zsuzsanna Darula, Attila Szorcsik, Ferenc Matyuska, Tibor Páli, Tamás Gajda
, New J. Chem.
, 2017
, 41
, 808
- Novel uridin-2′-yl carbamates: synthesis, incorporation into oligodeoxyribonucleotides, and remarkable fluorescence properties of 2′-pyren-1-ylmethylcarbamate. Vladimir A. Korshun, Dmitry A. Stetsenko, Michael J. Gait
, J. Chem. Soc., Perkin Trans. 1
, 2002
, 1092