专利号:US-7109377-B2 优先权日:1996-10-16 标 题:Synthesis of combinatorial libraries of compounds reminiscent of natural products 发明人:SCHREIBER STUART L; SHAIR MATTHEW D; TAN DEREK S; FOLEY MICHAEL A; STOCKWELL BRENT R 权利人:HARVARD COLLEGE 摘要:The present invention provides complex compounds reminiscent of natural products and libraries thereof, as well as methods for their production. The inventive compounds and libraries of compounds are reminiscent of natural products in that they contain one or more stereocenters, and a high density and diversity of functionality. In general, the inventive libraries are synthesized from diversifiable scaffold structures, which are synthesized from readily available or easily synthesizable template structures. In certain embodiments, the inventive compounds and libraries are generated from diversifiable scaffolds synthesized from a shikimic acid based epoxyol template. In other embodiments, the inventive compounds and libraries are generated from diversifiable scaffolds synthesized from the pyridine-based template isonicotinamide. The present invention also provides a novel ortho-nitrobenzyl photolinker and a method for its synthesis. Furthermore, the present invention provides methods and kits for determining one or more biological activities of members of the inventive libraries. Additionally, the present invention provides pharmaceutical compositions containing one or more library members.
专利号:US-2003082830-A1 优先权日:1996-10-16 标 题:Synthesis of combinatorial libraries of compounds reminiscent of natural products
专利号:WO-0006525-A9 优先权日:1998-07-25 标题:Synthesis of combinatorial libraries of compounds reminiscent of natural products
专利号:WO-0006525-A2 优先权日:1998-07-25 标 题:Synthesis of combinatorial libraries of compounds reminiscent of natural products
专利号:US-6448443-B1 优先权日:1996-10-16 标 题:Synthesis of combinatorial libraries of compounds reminiscent of natural products
专利号:RU-2071962-C1 优先权日:1987-12-18 标题 :Method of synthesis of triazolo-[4,3-a]-[1,4]-diazepines
参考标题:Facile Solid-Phase Ruthenium Assisted Azide-Alkyne Cycloaddition (Ruaac) Utilizing The Cp∗rucl(Cod)-Catalyst 作者:Ebbe Engholm,Nicolai Stuhr-Hansen,Ola Blixt |发布日期:2017.6 摘要:The Ruthenium Assisted Azide-Alkyne Cycloaddition (Ruaac) Reaction Is A Well-Established Method For The Generation Of 1,5- And 1,4,5-Substituted 1,2,3-Triazoles, Which We Have Extended To The Solid-Phase Synthesis Of 1,2,3-Triazole-Peptides. The 1,2,3-Triazole Moieties Were Formed Upon The Reaction Of Alkynes With A Solid-Phase Bound Secondary Azide In The Presence Of The Cp∗rucl(Cod) Catalyst At Room
合成参考文献
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