甲酸甲酯置于sodium Hydroxide,Wang Resin-Pentylstyrene[5-Ph(4Me)]N-Me-Imidazole(1+)*cl(1-)体系中,用 四氢呋喃 用作溶剂,化学反应 1.5H,以41%的收率获得2-羟基-2-甲氧基乙酸甲酯 参考文献:Imidazole Based Solid-Supported Catalysts For The Benzoin Condensation 标题:Imidazole Based Solid-Supported Catalysts For The Benzoin Condensation 摘要:New Polymer-Supported Imidazolium Salts Have Been Synthesised,And Their Utility As Pre-Catalysts In The Benzoin Reaction Has Been Demonstrated. (C) 2005 Elsevier Ltd. All Rights Reserved. Doi:10.1016/j.Tetlet.2005.08.141
专利号:US-9969685-B2 优先权日:2016-09-28 标 题 :Enantioselective synthesis of pyrroloindole compounds 发明人:SCHMIDT MICHAEL ANTHONY 权利人:BRISTOL MYERS SQUIBB CO 摘要:Compounds according to formula (I) or (II), wherein R 1 , R 2 , and R 3 are as defined in the specification, are versatile intermediates for the synthesis of DNA minor groove binder-alkylators having a cyclopropapyrroloindole (CPI) or seco-CPI alkylating subunit.
专利号:US-4424389-A 优先权日:1981-04-30 标 题:Synthesis of 6-hydroxychroman-2-methanol derivatives 发明人:SAKITO YOJI 权利人:SUMITOMO CHEMICAL CO 摘要:A process for producing chroman, a compound of the formula, ##STR1## or an optically active compound thereof wherein R 2 , R 3 and R 4 are each a hydrogen atom or a C 1 -C 4 alkyl group, which comprises reacting a compound of the formula, ##STR2## or an optically active compound thereof wherein A is an aryl group and R 5 is a C 1 -C 4 alkyl group, with a compound of the formula, ##STR3## wherein R 1 is a C 1 -C 3 alkyl group, X is a halogen atom and R 2 , R 3 and R 4 are as defined above, to obtain a compound of the formula, ##STR4## or an optically active compound thereof wherein A, R 1 , R 2 , R 3 and R 4 are as defined above, reacting the resulting compound with methylmagnesium halide and then hydrolyzing to obtain the corresponding 4-aryl substituted 2-hydroxy-2-methylbutanal, or an optically active compound thereof, reducing the resulting compound to obtain a diol, or an optically active compound thereof, and then oxidizing the resulting compound to obtain a compound of the formula, ##STR5## or an optically active compound thereof wherein R 2 , R 3 and R 4 are as defined above, followed by reduction. n Chromans, the objective compounds of this invention, are an intermediate for the synthesis of tocopherols, particularly α-tocopherol.
专利号:US-8324417-B2 优先权日:2009-08-19 标题:Process for the preparation of (S)-2-amino-5-cyclopropyl-4,4-difluoropentanoic acid and alkyl esters and acid salts thereof 发明人:HART BARRY; DENER JEFF; GREEN MICHAEL; STANDEN MICHAEL; KOCIAN OLDRICH 权利人:HART BARRY; DENER JEFF; GREEN MICHAEL; STANDEN MICHAEL; KOCIAN OLDRICH; VIROBAY INC 摘要:The present invention relates to a process for the preparation of alkyl esters of (S)-2-amino-5-cyclopropyl-4,4-difluoropentanoic acid, which are intermediates useful in the synthesis of (S)—N-(1-cyanocyclopropyl)-5-cyclopropyl-4,4-difluoro-2-((S)-2,2,2-trifluoro-1-(4-fluorophenyl)ethylamino)pentanamide and related compounds, which are compounds that are cysteine protease inhibitors.
专利号:US-9718807-B2 优先权日:2012-06-05 标 题 :Synthesis of antiviral compound 发明人:SCOTT ROBERT WILLIAM; VITALE JUSTIN PHILIP; MATTHEWS KENNETH STANLEY; TERESK MARTIN GERALD; FORMELLA ALEXANDRA; EVANS JARED WAYNE 权利人:GILEAD PHARMASSET LLC 摘要:The present disclosure provides processes for the preparation of a compound of formula I: n nwhich is useful as an antiviral agent. The disclosure also provides compounds that are synthetic intermediates to compounds of formula I.
专利号:US-7205300-B2 优先权日:1997-12-31 标 题:Aryl fused azapolycyclic compounds 发明人:COE JOTHAM WADSWORTH; BROOKS PAIGE ROANNE PALMER 权利人:PFIZER 摘要:This invention is directed to compounds of the formula (I): n nand their pharmaceutically acceptable salts, wherein R 1 , R 2 , and R 3 are as defined herein; intermediates for the synthesis of such compounds, pharmaceutical compositions containing such compounds; and methods of using such compounds in the treatment of neurological and psychological disorders.
专利号:WO-2018064094-A1 优先权日:2016-09-28 标题:Enantioselective synthesis of pyrroloindole compounds
参考标题:Total Synthesis Of The Serine-Threonine Phosphatase Inhibitor Microcystin-La 作者:John M. Humphrey,James B. Aggen,A. Richard Chamberlin |发布日期:1996.1.1 摘要:Element Of The Cell. There Is A Diverse Group Of Toxic Natural Products That Inhibit Certain Phosphatases, Thereby Disrupting Normal Biochemical Pathways. These Toxins Can Be Useful For Dissecting The Individual Biochemical Pathways Associated With Each Of These Enzymes. This Article Describes The First Total Synthesis Of One Such Toxin, The Cyclic Heptapeptide Microcystin-La. The Synthesis Features A Convergent
合成参考文献
摘要:Poechlauer, P.; Zimmermann, A., Science of Synthesis: Catalytic Reduction in Organic Synthesis, (2017) 1, 331. 参考文献:10.1038/s41698-020-0121-2 摘要:Datta P, Dey M, Ataie Z, Unutmaz D, Ozbolat IT. 3D bioprinting for reconstituting the cancer microenvironment. npj Precision Oncology. 2020 Jul 27;4(1):18. doi: 10.1038/s41698-020-0121-2.