372486-18-5Relevant articles and documents
Platinum complexes with anti-tumor activity and production method of platinum complexes with anti-tumor activity
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Paragraph 0041; 0043; 0046-0047, (2020/01/03)
The invention discloses platinum complexes with anti-tumor activity, and relates to the technical field of platinum complexes. The platinum complexes with anti-tumor activity comprise a complex A anda complex B, wherein with resorcinol as an initial raw m
Application of paeonol derivatives with vasodilator activity
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Paragraph 0028; 0035-0037, (2018/12/13)
The invention provides application of paeonol derivatives with vasodilator activity. The method comprises the following steps: carrying out a methylation reaction of 2,4-dihydroxyphenylpentanone underalkaline conditions, sequentially extracting and drying
Primulin derivative as well as synthesis method and application of primulin derivative
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Paragraph 0015, (2018/01/11)
The invention discloses a primulin derivative with antibacterial activity shown as the structural general formula (I), wherein R is selected from C2-C20 alkyls. The primulin derivative is prepared from raw materials including m-dihydroxybenzene and a fatty acid derivative by the steps: carrying out Friedel-Crafts acylation and methylation to synthesize a paeonol derivative, and carrying out oxidization after carrying out carbonyl reduction. The primulin derivative has good antibacterial activity and can be used as a potential antibacterial agent.
Synthesis and lipase-mediated stereoselective deacetylation of (±)-3-acetoxymethyl-3-alkyl-7-methoxychroman-4-ones
Poonam,Prasad, Ashok K,Azim, Abul,Kumar, Rajesh,Jain, Subhash C,Parmar, Virinder S,Olsen, Carl E,Errington, William
, p. 7395 - 7402 (2007/10/03)
Six (±)-3-acetoxymethyl-3-alkyl-7-methoxychroman-4-ones have been synthesized in four steps starting with the coupling of resorcinol with corresponding aliphatic acid leading to the formation of 2,4-dihydroxyphenyl alkyl ketones, which upon monomethylation and hydroxymethylation, followed by acetylation afforded the racemic acetoxymethylated compounds in 17-30% overall yields. Candida rugosa lipase-catalyzed deacetylation of (±)-3-acetoxymethylchromanones in diisopropyl ether exhibited fairly moderate enantioselectivity.