73220-34-5Relevant academic research and scientific papers
Zn(OTf)2-Catalyzed Formal [3 + 3] Cascade Annulation of Propargylic Alcohols with 2-Aminochromones: Accessing the Chromeno[2,3- b]pyridines
Tong, Pei,Sun, Zhou,Wang, Shutao,Zhang, Yuan,Li, Ying
, p. 13967 - 13974 (2019/10/16)
A Zn(OTf)2-catalyzed formal [3 + 3] cascade annulation strategy for the synthesis of functionalized chromeno[2,3-b]pyridines has been developed using propargylic alcohols and 2-aminochromones as the substrates. The protocol provides a convenien
Novel Flavonoids Derivative, its Preparation Method and Composition Comprising the Same
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Paragraph 0127; 0139; 0145; 0146, (2018/10/16)
The present invention relates to a novel flavonoid derivative, a preparation method thereof, and a cosmetic composition or a composition for external application for skin containing the novel flavonoid derivative as an active ingredient. The novel flavono
A Concise Synthesis of Pyrazole Analogues of CombretastatinA1 as Potent Anti-Tubulin Agents
Zaninetti, Roberta,Cortese, Salvatore V.,Aprile, Silvio,Massarotti, Alberto,Canonico, Pier Luigi,Sorba, Giovanni,Grosa, Giorgio,Genazzani, Armando A.,Pirali, Tracey
supporting information, p. 633 - 643 (2013/08/22)
CombretastatinA1 (CA1) binds to the β-subunit at the colchicine binding site of tubulin and inhibits polymerization. As such, it is both an antitumor agent and a vascular disrupting agent. It has been shown to be at least tenfold more potent than combreta
