专利号:US-9771379-B2 优先权日:2015-09-24 标题:N-(2-(2-amino-6-substituted-4,4a,5,6-tetrahydropyrano[3,4-d][1,3]OXAZIN-8a(8H)-yl)-thiazol-4-yl) amides 发明人:BRODNEY MICHAEL AARON; BUTLER CHRISTOPHER RYAN; ZHANG LEI; O'NEILL BRIAN THOMAS 权利人:PFIZER 摘要:The present invention is directed to compounds, tautomers and pharmaceutically acceptable salts of the compounds which are disclosed, wherein the compounds have the structure of Formula I, n nwherein the variables R 1 , R 2 , R 3 , R 4 and X are as defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.
专利号:US-9744173-B2 优先权日:2014-04-10 标题 :2-amino 6-methyl-4,4a,5,6-tetrahydropyrano[3,4-d][1,3]thiazin-8a(8H)-yl-1,3-thiazol-4-yl amides 发明人:BRODNEY MICHAEL AARON; BECK ELIZABETH MARY; BUTLER CHRISTOPHER RYAN; ZHANG LEI; O'NEILL BRIAN THOMAS; BARREIRO GABRIELA; LACHAPELLE ERIK ALPHIE; ROGERS BRUCE NELSEN 权利人:PFIZER 摘要:The present invention is directed to compounds, tautomers and pharmaceutically acceptable salts of the compounds which are disclosed, wherein the compounds have the structure of Formula I, n nand the variable R 1 is as defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.
专利号:US-9198917-B2 优先权日:2012-12-11 标题:Hexahydropyrano[3,4-d][1,3]thiazin-2-amine compounds 发明人:BRODNEY MICHAEL AARON; BECK ELIZABETH MARY; BUTLER CHRISTOPHER RYAN; DAVOREN JENNIFER ELIZABETH; O'NEILL BRIAN THOMAS 权利人:PFIZER 摘要:The present invention provides compounds of Formula I, and the tautomers thereof, and the pharmaceutically acceptable salts of the compounds and tautomers, wherein the compounds have the structure n nwherein the variables R 1 , R 2 , R 3 , R 4 and x are as defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.
专利号:CN-112979605-A 优先权日:2021-03-03 标题:A kind of stable isotope labeled zearalenone and its synthesis method
参考标题:Enantioselective Synthesis Of The 3C-Protease Inhibitor (-)-Thysanone By A Staunton-Weinreb Annulation Strategy 作者:Margaret Brimble,Jonathan Sperry,Tsz Yuen |发布日期:2009.8 摘要:The Total Synthesis Of (-)-Thysanone Is Described. The Key Step Involves The Addition Of An O-Toluate Anion To A Lactone To Create The Naphthopyran Framework (Staunton-Weinreb Annulation). This Synthesis Further Confirms The Absolute Stereochemistry Of The Natural Product To Be 1R,3S. Thysanone - Staunton-Weinreb Annulation - Total Synthesis - Natural Products - Polycycles
合成参考文献
摘要:Bartels, F.; Zimmer, R.; Christmann, M., Science of Synthesis Knowledge Updates, (2017) 3, 243. 摘要:Margaretha, P., Science of Synthesis Knowledge Updates, (2014) 2, 431. 摘要:Carter, R. G.; Kuiper, D. L., Science of Synthesis: Stereoselective Synthesis, (2011) 2, 886.