氯乙烯置于magnesium体系中,用 四氢呋喃 作为反应溶剂,化学反应 0.75H,反应生成 乙烯基氯化镁 参考文献:十九世纪sila-Pharmaka.sila-Pridinol和pridinol:Darstellung和eigenschaften Sowie Strukturen Im Kristallinen和gelöstenzustand 标题:十九世纪sila-Pharmaka.sila-Pridinol和pridinol:Darstellung和eigenschaften Sowie Strukturen Im Kristallinen和gelöstenzustand 摘要:Sila-Pridinol(2B),Eila Sila-Analogon Des Anticholinergicums Pridinol(2A),Wurde Auf Zwei Verschiedenen Wegen Dargestellt.die Kristall-Undmolekülstrukturenvon 2A和2B Wurdenrönt-Genstrukturanalytischbestimmt.2A Bildet Im Festen Zustand分子内wasserstoffbrückenbindungenaus,Währendsich In Kristallinem 2B Zentrosymmetrische,Durch Intermolekulareh-Brückenbindungenverknüpftecyclische Dimere Finden.2B Bildet Im DOI:10.1002/cber.19801130531
专利号:US-10053406-B2 优先权日:2015-10-23 标题 :Synthesis of honokiol 发明人:JARACZ STANISLAV; KOZLOWSKI MARISA; EUN LEE YOUNG; KIM SUN MIN 权利人:COLGATE PALMOLIVE CO; UNIV PENNSYLVANIA 摘要:Disclosed herein are improved methods for the synthesis of honokiol, as well as methods for the synthesis of 3,3′-di-tert-butyl-5,5′-dimethyl-[1,1′-biphenyl]-2,4′-diol, 3′,5-dimethyl-[1,1′-biphenyl]-2,4′-diol, and 2,4′-dimethoxy-3′,5-dimethyl-1,1′-biphenyl, 3,3′,5,5′-tetra-tert-butyl-[1,1′-biphenyl]-2,4′-diol, and certain tetrasubstituted bisphenols, and uses therefor.
专利号:US-8269001-B2 优先权日:2005-10-05 标题 :Process for the synthesis of HMG-CoA reductase inhibitors 发明人:CASAR ZDENKO 权利人:CASAR ZDENKO; LEK PHARMACEUTICALS 摘要:A novel synthesis of statins uses Wittig reaction of a heterocyclic core of statin with a lactonized side chain already possessing needed stereochemistry. Any separation of diastereoisomers is performed early in the course of synthesis.
专利号:US-4311645-A 优先权日:1980-03-24 标 题 :Synthesis of SRS-active compounds 发明人:ROSENBERGER MICHAEL 权利人:HOFFMANN LA ROCHE 摘要:A chemical synthesis of an SRS-A active compound from the reaction product of 1-halo-2-octyne and the ether of 2-penten-4-yn-1-ol including intermediates in the synthesis, some of which being antagonists of SRS-A useful for treating allergic reactions.
专利号:US-5847185-A 优先权日:1997-11-21 标题 :C-15 phosphonate reagent compositions and methods of synthesizing the same 发明人:BABLER JAMES H 权利人:LOYOLA UNIVERSITY OF CHICAGE 摘要:Allenic phosphonate reagent compositions are described which have the formula: ##STR1## wherein R and R'=C 1 -C 4 alkyl groups, or R, R'=(CH 2 ) n (n=2 or 3) or CH 2 C(CH 3 ) 2 CH 2 !. n Also described are methods for forming such allenic phosphonates from ethynyl-β-ionol, and for converting these allenic compounds to allylic phosphonate compounds which can be used in the synthesis of a variety of biologically-active materials.
专利号:US-4045452-A 优先权日:1974-03-13 标题 :Steroid total synthesis process utilizing a cyanoalkyl A-ring precursor 发明人:COHEN NOAL; ROSENBERGER MICHAEL; SAUCY GABRIEL 权利人:HOFFMANN LA ROCHE 摘要:A multi-step, stereospecific total synthesis of steroids utilizing intermediates having a cyanoalkyl A-ring precursor is disclosed. The initial starting materials for this process are the relatively inexpensive and commercially available reagents γ-butyrolactone and sodium cyanide. The process is suitable for the preparation of racemic or optically active, medicinally valuable steroids, particularly 19-norsteroids. It is a feature of this process that conditions employed during the multiple step synthesis are selected so as to retain the normally labile nitrile group even during hydrogenation and hydrolysis steps. In this manner, it is possible to employ the nitrile group as an A-ring precursor without resorting to protective groups as wasl heretofore found necessary in previous steroid total synthesis processes.
专利号:US-4105676-A 优先权日:1975-12-22 标题 :Steroid total synthesis process utilizing a cyanoalkyl a-ring precursor 发明人:COHEN NOAL; ROSENBERGER MICHAEL; SAUCY GABRIEL 权利人:HOFFMANN LA ROCHE 摘要:A multi-step, stereospecific total synthesis of steroids utilizing intermediates having a cyanoalkyl A-ring precursor is disclosed. The initial starting materials for this process are the relatively inexpensive and commercially available reagents γ-butyrolactone and sodium cyanide. The process is suitable for the preparation of racemic or optically active, medicinally valuable steroids, particularly 19-norsteroids. It is a feature of this process that conditions employed during the multiple step synthesis are selected so as to retain the normally labile nitrile group even during hydrogenation and hydrolysis steps. In this manner, it is possible to employ the nitrile group as an A-ring precursor without resorting to protective groups as was heretofore found necessary in previous steroid total synthesis processes.