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    • 36. 发明申请
    • NOVEL SIRTUIN ACTIVATING COMPOUNDS AND METHODS FOR MAKING THE SAME
    • 新型SIRTUIN激活化合物及其制备方法
    • WO2005069998A2
    • 2005-08-04
    • PCT/US2005/002229
    • 2005-01-19
    • BRIGHAM YOUNG UNIVERSITY TECHNOLOGY TRANSFER OFFICEANDRUS, Merritt, B.LIU, Jing
    • ANDRUS, Merritt, B.LIU, Jing
    • C07C67/08C07C67/29C07C67/293C07C69/017
    • C07C69/017C07C67/08C07C67/14C07C67/287C07C67/29C07C67/293Y02P20/55C07C69/716C07C69/63C07C69/18C07C69/16
    • The present invention includes methods for preparing resveratrol, resveratrol esters and substituted and unsubstituted stilbenes of the formula given below; where each Y is -O or halogen, each Z is -O or halogen, each n and each m is independently the value of 0, 1, 2, 3, 4 or 5, each A and each B is independently selected from P n , R or absent, each V and each W is independently selected from P n , straight or branched alkyl of from (2) to (6) carbon atoms and cycloalkyl of from (3) to (8) carbon atoms, alkoxy, phenyl, benzyl or halogen, R is independently selected from the group comprising alkyl with at least one carbon atom, aryl and aralkyl, P n is an alcohol protecting group and diastereoisomers of the foregoing. The compounds are made from a multi-step process including a N-heterocyclic carbene-type ligand coupling in the presence of a base with benzyol halide and styrene coupling partners. These compounds show increased stability for use in the food, cosmetic and pharmaceutical industries.
    • 本发明包括用于制备下列给出的式的白藜芦醇,白藜芦醇酯和取代和未取代的二苯乙烯的方法; 其中每个Y是-O或卤素,每个Z是-O或卤素,每个n和每个m独立地是0,1,2,3,4或5的值,每个A和每个B独立地选自Pn, R或不存在,每个V和每个W独立地选自(2)至(6)个碳原子的直链或支链烷基,(3)至(8)碳原子的烷基,烷氧基,苯基,苄基或 卤素,R独立地选自烷基与至少一个碳原子的基团,芳基和芳烷基,Pn是醇保护基和前述的非对映异构体。 所述化合物由多步法制备,包括在碱存在下与苄氧基卤化物和苯乙烯偶合物偶联的N-杂环卡宾型配体偶联。 这些化合物在食品,化妆品和制药工业中显示出增加的稳定性。
    • 40. 发明申请
    • PREPARATION OF (R)-2-ALKYL-3-PHENYLPROPIONIC ACIDS.
    • (R)-2-烷基-3-苯基丙酸的制备。
    • WO02002500A1
    • 2002-01-10
    • PCT/CH2001/000397
    • 2001-06-26
    • B01J31/24C07B53/00C07B61/00C07C51/36C07C59/64C07C59/66C07C62/34C07C67/293
    • C07C59/66C07C51/36
    • Compounds of formula (I), wherein R1 and R2 are, independently of one another, H, C1-C6alkyl, C1-C6halogenalkyl, C1-C6alkoxy, C1-C6alkoxy-C1-C6alkyl, or C1-C6alkoxy-C1-C6alkyloxy, and R3 is C1-C6alkyl, are obtainable in high yields by stereoselective addition of R3-substituted propionic acid esters to R1- and R2-substituted benzaldehydes of formula R-CHO to form corresponding 3-R-3-hydroxy-2-R3-propionic acid esters, conversion of the OH group to a leavaing group, subsequent regioselective elimination to form 3-R-2-R3-propenic acid esters, and their hydrolysis to form corresponding propenic carboxylic acids and their enantioselective hydrogenation, wherein R is (a).
    • 式(I)化合物,其中R 1和R 2彼此独立地为H,C 1 -C 6烷基,C 1 -C 6卤代烷基,C 1 -C 6烷氧基,C 1 -C 6烷氧基-C 1 -C 6烷基或C 1 -C 6烷氧基-C 1 -C 6烷氧基, R 3是C 1 -C 6烷基,可以通过立体选择性地将R 3取代的丙酸酯加成到式R-CHO的R 1和R 2取代的苯甲醛以高产率获得,形成相应的3-R-3-羟基-2-R3-丙酸 酸酯,OH基转化为脱氯基团,随后进行区域选择性消除以形成3-R-2-R3-丙烯酸酯,并且它们的水解形成相应的丙烯羧酸及其对映选择性氢化,其中R为(a) 。