化学
查尔酮
香兰素
溴化物
醋酸酐
三氟化硼
醋酸
酰化
产量(工程)
溴化氢
有机化学
去甲基化
羟醛缩合
药物化学
酒
醌
催化作用
生物化学
材料科学
DNA甲基化
基因表达
冶金
溴
基因
作者
Koteswara R. Kamma,Joungmo Cho,Hyo Jun Won,Sang-Yeol Nam,Ngan Hong Le,Je Hyeong Jung,Kee‐In Lee
出处
期刊:Molecules
[MDPI AG]
日期:2024-01-19
卷期号:29 (2): 513-513
被引量:1
标识
DOI:10.3390/molecules29020513
摘要
During the synthetic studies toward 5,6,7,3',4'-monomethoxytetrahydroxyflavones, a concise pedalitin synthesis procedure was achieved. As previously reported, 6-hydroxy-2,3,4-trimethoxyacetophenone was prepared by Friedel-Crafts acylation of 1,4-dihydroxy-2,6-dimethoxybenzene with boron trifluoride diethyl etherate in acetic acid. When aldol condensation of 6-hydroxy-2,3,4-trimethoxyacetophenone
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