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    • 1. 发明授权
    • Supramolecular pairing system, its preparation and use
    • 超分子配对体系,其制备和应用
    • US06689884B1
    • 2004-02-10
    • US09509040
    • 2000-08-03
    • Christian MiculkaNorbert WindhabAlbert EschenmoserStefan SchererGerhard Quinkert
    • Christian MiculkaNorbert WindhabAlbert EschenmoserStefan SchererGerhard Quinkert
    • C07D23900
    • C12Q1/68
    • The invention relates to a compound of formula (I), wherein R1 is NR3R4, OR3 or SR3 with R3 and R4 being H or CnH2n+1 independently of each other and being the same or different, n being a whole number from 1 to 12; R2 is equal to CmH2m—C(X)—Y with X being ═O, ═S or ═N, Y being equal to OR3, NR3R4 or SR3, R3 and R4 having the same meaning given above, and m being a whole number from 1 to 4; or R2 is equal to CmH2m—Z—Y′ with Z being a sulfonyl, phosphonyl, ether or amine group, Y′ being equal to H, CnH2n+1, OR3, NR3R4 or SR3 then Z is sulphonyl or phosphonyl group, n, R3 and R4 having the meaning given above, and Y′ being equal to CnH2n+1 when Z is an ether or an amine group; A, B, and D are the same or different and mean CR5R6, O, NR7 ou S independently of each other with R5, R6 and R7 being H or CnH2n+1, independently of each other, n having the meaning given above; and C is equal to CR8 or N with R8 having the meaning of R5 independently, A—B, B—C or C—D not being two identical heteroatoms; and nucleobase means thymine, uracile, adenine, cytosine, guanine, isocytosine, isoguanine, xanthine or hypoxanthine. The invention also relates to a method for producing these derivatives and to their use in pairing and/or testing systems.
    • 本发明涉及式(I)化合物,其中R 1为NR 3 R 4,OR 3或SR 3,R 3和R 4为H或C n H 2n +1彼此独立且相同或不同,n为1至12的整数; R 2等于CmH2m-C(X)-Y,其中X为= O,= S或= N,Y等于OR 3,NR 3 R 4或SR 3, R 3和R 4具有上述相同的含义,m为1至4的整数; 或R 2等于C m H 2 m-Z Y',其中Z是磺酰基,膦酰基,醚或胺基,Y'等于H,C n H 2n + 1,OR 3,NR 3 R 4或 当Z为醚或胺基时,Z为磺酰基或膦酰基,n,R 3和R 4具有上述含义,Y'等于C n H 2n + 1; A,B和D相同或不同,并且R 5,R 6和R 7独立地为CR 5,R 6和R 7独立地为CR 5 R 6,O,NR 7 H或C n H 2n + 1彼此独立地具有上述含义的n; 并且C等于CR 8或N,其中R 8独立地具有R 5的含义,A-B,B-C或C-D不是两个相同的杂原子; 核碱基是指胸腺嘧啶,尿嘧啶,腺嘌呤,胞嘧啶,鸟嘌呤,异胞嘧啶,异鸟嘌呤,黄嘌呤或次黄嘌呤。 本发明还涉及一种制备这些衍生物的方法及其在配对和/或测试系统中的用途。
    • 7. 发明授权
    • Method for the production of aldehydes and ketones by oxidizing primary and secondary alcohols with alkylphosphonic acid anhydrides
    • 通过用烷基膦酸酐氧化伯醇和仲醇生产醛和酮的方法
    • US07262328B1
    • 2007-08-28
    • US10592439
    • 2005-04-18
    • Andreas MeudtStefan SchererClaudius Boehm
    • Andreas MeudtStefan SchererClaudius Boehm
    • C07C45/38C07C45/39
    • C07C45/29C07B41/06C07C269/06C07C47/21C07C47/54C07C49/10C07C271/22
    • The invention relates to a method for the production of a.) aldehydes of formula (II): R1—CHO and b.) aldehydes of formula (III): R1—C(O)—R2 by reacting a.) primary alcohols (R1CH2—OH) or b.) secondary alcohols (R1—CH(OH)—R2) with cyclic phosphonic acid anhydrides in the presence of dialkyl-, diaryl- and/or alkyl-aryl sulphonic oxides at a temperature in the region of between −100 to +120° C., whereby R1 and/or R2 represent H, a substituted linear or branched C1-C12-alkyl radical, a substituted C3-C10 cycloalkyl-, alkenyl-, aryl- or heteroaryl radical. A cyclic phosphonic acid anhydride is used, preferably, as a 2,4,6-substituted 1,3,5,2,4,6-trioxatriphosphinane of formula (I), wherein R′ independently represents allyl, aryl or open-chained or branched C1-C12-alkyl-radicals. Optionally, the reaction can be carried out in the presence of a tertiary amine base NR53
    • 本发明涉及一种制备式(II)的醛的方法:R 1 -CHO和b)式(III)的醛:R 1〜 通过使a。)伯醇(R 1 CH 2 CH 2 -OH)或b。)二级(C 1 -C 4) 在二烷基 - ,二芳基 - 和/或烷基 - 芳基磺酸氧化物的存在下,与环状膦酸酐反应,得到醇(R 1 -CH 2(OH)-R 2) 在-100至+ 120℃之间的区域中的温度,其中R 1和/或R 2表示H,取代的直链或支链C 1〜 取代的C 3 -C 10 - 环烷基 - ,链烯基 - ,芳基 - 或杂芳基(C 1 -C 6) 激进。 优选使用环状膦酸酐作为式(I)的2,4,6-取代的1,3,5,2,4,6-三氧杂三磷杂环己烷,其中R'独立地表示烯丙基,芳基或开链 或支链C 1 -C 12 - 烷基 - 基团。 任选地,反应可以在叔胺碱NR 5 SO 3存在下进行,
    • 8. 发明授权
    • Method for producing (1,1′,4, 11″)-terphenyl compounds
    • 生产(1,1',4,11“) - 三联苯化合物的方法
    • US06762315B1
    • 2004-07-13
    • US09914478
    • 2001-08-24
    • Stefan SchererSteffen Haber
    • Stefan SchererSteffen Haber
    • C07C6976
    • C07C67/343C07C69/76
    • The invention relates to a method for producing [1,1′:4′,1″]-terphenyl compounds of the formula which comprises reacting a metal aryl of the formula with a boric ester at −80 to 40° C. in the presence of an inert solvent, converting the reaction product by hydrolysis into a boronic acid of the formula reacting the boronic acid, a boronic anhydride obtainable from boronic acid by elimination of water, or a mixture of boronic acid and boronic anhydride, with an alcohol, and reacting the boronic ester formed thereby with a biphenyl compound of the formula at 40 to 180° C. in the presence of a catalyst, of an acid-binding agent and of a polar solvent.
    • 本发明涉及一种生产该配方的[1,1':4',1“] - 三联苯化合物的方法,包括在-80至40℃下在-80至40℃下,在存在下使硼酸酯的金属芳基 惰性溶剂,通过水解将反应产物转化成硼酸的硼酸,通过除去水从硼酸获得的硼酸酐,或硼酸和硼酸酐的混合物与醇反应,并使 在催化剂存在下,在酸结合剂和极性溶剂的存在下,由式40至180℃的联苯化合物形成硼酸酯。