专利号:WO-2009115333-A1 优先权日:2008-03-20 标 题:Novel synthesis of praziquantel 发明人:DOEMLING ALEXANDER 权利人:DOEMLING ALEXANDER 摘要:The present invention discloses a novel and efficient synthesis of praziquantel (I).
专利号:WO-2017082924-A1 优先权日:2015-11-13 标题 :Peptide and peptide mimetic binding antagonists of polo-like kinase 1 polo box domain and methods of use 发明人:BURKE TERRENCE R JR; HYMEL DAVID 权利人:THE US SECRETARY DEPT OF HEALTH & HUMAN SERVICES 摘要:The description provides novel compounds that may serve as anticancer therapeutics. The compounds of the description bind to polo-like kinases through the polo-box domain. The peptide derivatives of the description have achieved improved efficacy in biochemical assays against Plk1. The description also provides methods of use, methods of preparation, compositions, and kits thereof. Further, the description provides a novel method of design and/or synthesis of phosphoryl-derived peptide derivatives useful as therapeutic agents.
专利号:US-2023357286-A1 优先权日:2020-07-24 标 题:Ketone synthesis and applications 发明人:KISHI YOSHITO; UMEHARA ATSUSHI 权利人:HARVARD COLLEGE 摘要:Provided are new nickel./zirconium-mediated coupling reactions useful in the synthesis of ketone-containing compounds, e.g., halichondrin natural products and related molecules. A feature of the present disclosure is the use of a nickel(I) catalyst in tandem with a nickel (II) catalyst in the Ni/Zr-mediated coupling reactions. Without wishing to be bound by any particular theory, the nickel (I) catalyst selectively activates the electrophilic coupling partner (i.e., the compound of Formula (A)), and the nickel(ll) catalyst selectively activates the nucleophilic coupling partner (i.e., a thioester of Formula (B)). This dual catalyst system leads to improved coupling efficiency and eliminates the need for a large excess of one of the coupling partners (i.e., a compound of Formula (A) or (B)).
专利号:US-4033949-A 优先权日:1976-04-14 标 题:Analogs of thromboxane B2 and processes for their synthesis 发明人:KELLY ROBERT C; NELSON NORMAN A 权利人:UPJOHN CO 摘要:The present specification provides novel intermediates and novel processes for the synthesis of various side chain and skeletal analogs of Thromboxane B 2 (11β-homo-11a-oxa-PGF 2 .sub.α). These analogs are particularly and especially useful as reproductive cycle control agents.
专利号:US-2008183007-A1 优先权日:2004-10-08 标 题 :Process For the Preparation of Alkyl Phosphinic Acids 发明人:THELIN MATS 权利人:ASTRAZENECA AB 摘要:The present invention relates to a new process for the synthesis of alkyl phosphinic acids, and more particularly to a coupling reaction between an alkylhalide and a hypophosphorous acid derivative by a radical initiated reaction. The invention also relates to compounds obtainable by the method of the invention.
专利号:US-2015158020-A1 优先权日:2013-12-11 标题:Synthesis of zeolites using an organoammonium compound 发明人:NICHOLAS CHRISTOPHER P; MILLER MARK A 权利人:UOP LLC 摘要:A method for synthesizing a zeolite includes the steps of: (a) preparing an aqueous mixture comprising water, a substituted hydrocarbon and an amine; (b) reacting the aqueous mixture; (c) obtaining a solution comprising an organoammonium product; (d) forming a reaction mixture including reactive sources of M, Al, Si, optionally seeds of a layered material L, and the solution, wherein M is a metal; and (e) heating the reaction mixture to form the zeolite. The substituted hydrocarbon can be an α,ω-dihalogen substituted alkane, and the amine is preferably essentially incapable of undergoing pyramidal inversion.
参考标题:Organocerium Additions To Proline-Derived Hydrazones: Synthesis Of Enantiomerically Enriched Amines 作者:Scott E. Denmark,James P. Edwards,Theodor Weber,David W. Piotrowski |发布日期:2010.5 摘要:The Addition Of Organocerium Reagents (From Both Organolithium And Organomagnesium Precursors) To Chiral Aldehyde Hydrazones Prepared From 1-Aminoproline Derivatives Has Been Studied. The Additions Proceed In Good Yield And High Diastereoselectivity And With Good Nucleophile (Me, N-Bu, I-Pr, T-Bu, Ph, Etc.) And Substrate Scope (Alkyl, Alkenyl And Aryl). The Resulting Hydrazines Can Be Converted To
合成参考文献
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