GB522531A - - Google Patents

Info

Publication number
GB522531A
GB522531A GB522531DA GB522531A GB 522531 A GB522531 A GB 522531A GB 522531D A GB522531D A GB 522531DA GB 522531 A GB522531 A GB 522531A
Authority
GB
United Kingdom
Prior art keywords
methyl
aminopyrimidine
ethoxymethyl
dec
prepared
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
Other languages
English (en)
Publication date
Publication of GB522531A publication Critical patent/GB522531A/en
Expired legal-status Critical Current

Links

Landscapes

  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
GB522531D Expired GB522531A (US07608600-20091027-C00054.png)

Publications (1)

Publication Number Publication Date
GB522531A true GB522531A (US07608600-20091027-C00054.png) 1900-01-01

Family

ID=1748019

Family Applications (1)

Application Number Title Priority Date Filing Date
GB522531D Expired GB522531A (US07608600-20091027-C00054.png)

Country Status (1)

Country Link
GB (1) GB522531A (US07608600-20091027-C00054.png)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1150987B (de) * 1960-07-28 1963-07-04 Knoll Ag Verfahren zur Herstellung von 2-Methyl-4-amino-5-chlormethyl-pyrimidin-hydrochlorid
DE1294384B (de) * 1959-11-20 1969-05-08 Merck & Co Inc Verfahren zur Herstellung von 1-(2-Alkyl-4-amino-5-pyrimidyl-methyl)-pyridiniumhalogeniden

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1294384B (de) * 1959-11-20 1969-05-08 Merck & Co Inc Verfahren zur Herstellung von 1-(2-Alkyl-4-amino-5-pyrimidyl-methyl)-pyridiniumhalogeniden
DE1150987B (de) * 1960-07-28 1963-07-04 Knoll Ag Verfahren zur Herstellung von 2-Methyl-4-amino-5-chlormethyl-pyrimidin-hydrochlorid

Similar Documents

Publication Publication Date Title
JPH06287173A (ja) L−形1:1金属メチオニン錯体
Tronche et al. Polar substituent and solvent effects on the kinetics of radical reactions with thiols
ES2190794T3 (es) Procedimiento para la preparacion de disoluciones acuosas de dioxido de cloro.
Wynne et al. Physiological studies on spore germination, with special reference to Clostridium botulinum: III. Carbon dioxide and germination, with a note on carbon dioxide and aerobic spores
KR101443429B1 (ko) 히알루론산의 제조 방법
Flood et al. Pigments of Pseudomonas species. Part V. Biosynthesis of pyocyanin and the pigments of Ps. aureofaciens
Beach et al. Investigations of structures of substituted lumazines by deuterium exchange and nuclear magnetic resonance spectroscopy
GB522531A (US07608600-20091027-C00054.png)
Wiame et al. Oxidative assimilation by Pseudomonas saccharophila with C14-labeled substrates
Subbarow et al. Pantothenic acid as a factor in rat nutrition
CN108017561A (zh) 一种精制卡谷氨酸的方法
MITSUDA et al. BIOGENESIS OF RIBOFLAVIN IN GREEN LEAVES III. ON ENZYMATIC CONVERSION OF 6, 7-DIMETHYL-8-RIBITYLLUMAZINE TO RIBOFLAVIN AND 6-METHYL-8-RIBITYL-2, 4, 7-TRIOXO-HEXAHYDROPTERIDINE
Riley et al. Metabolism of ciliary body in relation to formation of aqueous humour
US3058888A (en) Process for producing alpha-isoleucine
EP1142578B1 (en) Method for producing an antitumoral agent and antitumoral agent thus obtained
Trudinger The synthesis of indole from anthranilic acid by Escherichia coli
KUWADA et al. On the biosynthesis of riboflavin in the culture of Eremothecium ashbyii
GB1384194A (en) Process for the production of trisodium or tripotassium citrate
US2457375A (en) Purification of pteroic acid amides
Wright Thymidine and vitamin B12
Kuwada et al. Supplement of the Notice on the Formation of 6-Methyl-7-hydroxyribolumazine.(Application of Chromatography. XLVI.)
JPH07194A (ja) 無細胞タンパク合成系によるタンパクの製造方法
DE59304476D1 (de) Lagerstabile Lösungen von carbonisiertem Magnesiumethylat in Ethanol sowie deren Herstellung und Verwendung
Whiteside-Carlson et al. Studies of the effect of para-aminobenzoic acid, folic acid, and sulfanilamide on dextran synthesis by leuconostoc
CN105624224A (zh) 一种以酶法结合膜技术生产d-盐酸半胱氨酸的方法