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    • 4. 发明授权
    • Cyclic acetals of N-acylglutamic acid-.gamma.-semialdehydes, process for
their production and use
    • N-酰基谷氨酸-γ-甲醛的环状缩醛,其生产和使用过程
    • US4424370A
    • 1984-01-03
    • US320129
    • 1981-11-10
    • Axel KleemannMarc Samson
    • Axel KleemannMarc Samson
    • C07D209/20C07D317/30C07D319/06C07D405/06
    • C07D209/20C07D317/30C07D319/06
    • The invention is directed to a cyclic acetal of N-acylglutamic acid-.gamma.-semialdehyde of the formula ##STR1## in which A is an unsubstituted alkylene group having 2 to 3 carbon atoms or such an alkylene group substituted by 1 to 2 methyl groups and R is a methyl, methoxy, phenyl, or benzyloxy group and to a method of producing a compound of formula (I) by reaction of a compound of the general formula ##STR2## in which A is as defined above, with hydrogen cyanide or a cyanide ion supplying compound, ammonia or an ammonium ion supplying compound and carbon dioxide or a carbonate ion supplying compound and basic hydrolysis of the reaction mixture obtained and reaction of the hydrolysis mixture with a suitable acylating compound and use of the compounds of formula (I) to produce .alpha.-N-acyltryptophane.
    • 本发明涉及式(I)的N-酰基谷氨酸-γ-甲醛的环状缩醛,其中A是未取代的具有2至3个碳原子的亚烷基或这样的被1至2个取代的亚烷基 甲基,R是甲基,甲氧基,苯基或苄氧基,并且通过使其中A定义如上所述的通式(IMAGE)(II)的化合物的反应制备式(I)化合物的方法 用氰化氢或氰化物离子供给化合物,氨或铵离子供给化合物和二氧化碳或碳酸根离子供给化合物进行碱性水解,得到的反应混合物与水解混合物与合适的酰化化合物反应,并使用 式(I)的化合物以产生α-N-酰基色氨酸。
    • 5. 发明授权
    • Process for the production of peptides
    • 生产肽的方法
    • US4374062A
    • 1983-02-15
    • US311454
    • 1981-10-14
    • Axel KleemannJurgen MartensMarc Samson
    • Axel KleemannJurgen MartensMarc Samson
    • C07K1/00B01J31/00C07C67/00C07C231/00C07C231/12C07C231/18C07K1/02C07K1/113C07K5/06C07C103/52
    • C07K1/023
    • There are produced peptides by asymmetrical hydrogenation of dehydropeptides of the general formula ##STR1## in which n is a whole number from 1 to 4, R.sub.1 and R.sub.2 are the same or different, and are hydrogen, a straight or branched chain alkyl group with 1 to 10 carbon atoms, or such a group substituted with a carboxyl group, a phenyl group which is unsubstituted or substituted in the 3 or 4 position or in both the 3 and 4 positions by a hydroxyl, alkoxy, or acyloxy group or an indolyl group which is unsubstituted or substituted in the 6 position by fluorine or chlorine or an indolyl group substituted by a methyl group. R.sub.3 is hydrogen, an alkali metal, or a lower alkyl group with 1 to 4 carbon atoms, R.sub.4 is hydrogen, an acetyl group or a chloroacetyl group and R.sub.5 is hydrogen or a straight or branched chain alkyl group having 1 to 4 carbon atoms with the proviso that when n is 2, 3, or 4, the individual groups R.sub.5 are the same or different, in the presence of chiral rhodium-complexes.
    • 通过非对称氢化产生通式为“IMAGE”的脱氢肽的肽,其中n为1至4的整数,R 1和R 2相同或不同,为氢,具有1个直链或支链烷基的直链或支链烷基 或被羧基取代的基团,未被取代或在3或4位或3或4位被羟基,烷氧基或酰氧基或吲哚基取代的苯基 其未被取代或在6位被氟或氯取代或被甲基取代的吲哚基。 R3是氢,碱金属或具有1至4个碳原子的低级烷基,R4是氢,乙酰基或氯乙酰基,R5是氢或具有1-4个碳原子的直链或支链烷基, 条件是当n为2,3或4时,在手性铑配合物的存在下,各基团R 5相同或不同。
    • 7. 发明授权
    • Aqueous solutions of sodium salts of trimercapto-s-triazine, their
preparation and use
    • 三巯基-s-三嗪的钠盐水溶液,其制备和用途
    • US5258515A
    • 1993-11-02
    • US932745
    • 1992-08-25
    • Klaus HentschelMarc SamsonMarcel VingerhoetsKarl-Ludwig Weber
    • Klaus HentschelMarc SamsonMarcel VingerhoetsKarl-Ludwig Weber
    • C07D251/38
    • C07D251/38
    • The invention relates to aqueous solutions of sodium salts of trimercapto-s-triazine whose molar saturation concentration at 0.degree. C. to 40.degree. C. is above the saturation concentration of trimercapto-s-triazine trisodium salt (TMT-Na.sub.3). More than two but less than three hydrogen atoms of the trimercapto-s-triazine are replaced by sodium ions. The solutions preferably contain trimercapto-s-triazine disodium salt (TMT-Na.sub.2) in addition to a little TMT-Na.sub.3. Surprisingly, the water solubility of TMT-Na.sub.2 is greater than that of TMT-Na.sub.3. The solutions represent a suitable supply form for the active substance trimercapto-s-triazine (TMT-H.sub.3) used in the separation of heavy metals The preparation takes place by means of reacting TMT-Na.sub.3 with TMT-H.sub.3 in a molar ratio of 1:greater than 0-less than 0.5, especially 1:0.1 to 1:
    • 本发明涉及三聚巯基三嗪的钠盐水溶液,其摩尔饱和浓度在0℃至40℃高于三巯基-s-三嗪三钠盐(TMT-Na 3)的饱和浓度。 三聚巯基-s-三嗪的多于两个但少于三个的氢原子被钠离子代替。 除了少量TMT-Na3之外,溶液优选含有三巯基-s-三嗪二钠盐(TMT-Na2)。 令人惊讶的是,TMT-Na2的水溶性大于TMT-Na3的水溶性。 该溶液代表用于分离重金属的活性物质三巯基-s-三嗪(TMT-H3)的合适供应形式。该制备通过使TMT-Na 3与TMT-H3以摩尔比1: 大于0-小于0.5,特别是在水溶液中为1:0.1至1:<0.5。