专利号:US-6252092-B1 优先权日:1999-04-30 标 题 :Process for synthesis of 5-alkylbenzodioxoles 发明人:BORZATTA VALERIO; BRANCALEONI DARIO; BATTISTINI CHRISTIAN 权利人:ENDURA SPA 摘要:The following description refers to a new process for the synthesis of 5-alkylated benzo[1,3]dioxole, comprising the following steps in sequence: catalytic hydrogenation of 4-acylphenol; acylation; displacement catalysed by Lewis acids; treatment with an inorganic basic compound and hydrogen peroxide; reaction with alkyl dihalides or dialkoxyalkanes. n The process described herein, which yields 5-alkylbenzo[1,3]dioxoles, is economic and can be easily scaled up to industrial size.
专利号:US-11746364-B2 优先权日:2018-01-17 标题 :Enzymatic synthesis of kavalactones and flavokavains 发明人:PLUSKAL TOMÃ?S; Weng jing-ke 权利人:WHITEHEAD INST BIOMEDICAL RES 摘要:Disclosed are methods, compositions, proteins, nucleic acids, cells, vectors, compounds, reagents, and systems for the preparation of kavalactones, flavokavains, and kavalactone and flavokavain biosynthetic intermediates using enzymes expressed in heterologous host cells, such as microorganisms or plants, or using in vitro enzymatic reactions. This invention also provides for the expression of the enzymes by recombinant cell lines and vectors. Furthermore, the enzymes can be components of constructs such as fusion proteins. The kavalactones produced can be utilized to treat anxiety disorder, insomnia, and other psychological and neurological disorders. The flavokavains produced can be utilized to treat various cancers including colon, bladder, and breast cancers.
专利号:WO-2013001830-A1 优先权日:2011-06-30 标题 :Nucleoside antibiotic derivative 发明人:ICHIKAWA SATOSHI; MATSUDA AKIRA; OKAMOTO KAZUYA; SAKAGAMI MASAHIRO 权利人:UNIV HOKKAIDO NAT UNIV CORP; SHIONOGI & CO; ICHIKAWA SATOSHI; MATSUDA AKIRA; OKAMOTO KAZUYA; SAKAGAMI MASAHIRO 摘要:The present invention addresses the problem of providing a new compound having antibacterial activity. Disclosed is a compound expressing antibacterial activity, more preferably an antibacterial nucleoside compound expressing antibacterial activity by inhibiting the activity of MraY, particularly a new derivative of Pacidamycin that is an MraY inhibitor. This new derivative of Pacidamycin or a pharmaceutically acceptable salt therof solve the abovementioned problem. By means of the method of the present invention, total synthesis of natural Pacidamycin D and its derivative is achieved.
专利号:WO-2012032085-A1 优先权日:2010-09-10 标题 :Synthesis of trivalent flexible frameworks with ligands comprising catechol units for functionalizing surfaces
专利号:CN-111254151-A 优先权日:2020-04-01 标 题 :A catechol 1,2-dioxygenase gene and its application in the synthesis of 4-position substituted cis, cis-muconic acid
专利号:WO-2012032084-A1 优先权日:2010-09-10 标 题:Synthesis of tripodal catechol derivatives having an adamantyl basic framework for functionalizing surfaces
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