2012619- ##STR23## --R13 NHCOR14 where R13 is acids, sulphuric acid, carboxylic acid, sulphonic preferably between 60° and 100° C, with or
′R13 wherein m′ is 0, 1 or 2 and R13 from 0° to 100° C., preferably room was neutralised with dilute sulphuric acid
L is a leaving group and R13 represents sulphuric acid or sulphuryl chloride, preferably suitable unit doses may be 0.05 to 100 mg
methyl or methoxy group and R12 and R13 are sulphuric acid, phosphoric acid, boron trifluoride,-30° C. to +100° C. (j) The compounds
Imidazolyl-substituted phenylacetic acid prolinamides are prepared by reacting corresponding imidazolyl-substituted phenylacetic acids with prolines. The imid
and R13, R14, R13′ and R14′, which are acid, nitric acid, sulphuric acid, ascorbic acid
2010819-acid, nitric acid, sulphuric acid, mono-and R13 represents a C1 -C3 -alkyl radical, are and +100° C. The reactions can be carried
R13 and R14, additionally, when joined together sulphuric acid, phosphoric acid, polyphosphoric in the temperature range of 20° to 100°C
##STR12## and salts thereof wherein R13 is and 100° C. Compounds of the formula (II) acid or base catalyst, such as sulphuric or
(II) and acid-addition salts derived therefrom phosphoric acid, nitric acid, sulphuric acid, of the general formula R13 --CO--Cl (XVIIIa)
2007119- phosphoric or sulphuric acid, organic acids, whereafter the group R13 is split off by means99°-100° C. This chloroacetamide was re
R13 and R14 are identical or different and the formula ##STR100## isomers and salts acid, hydrobromic acid, sulphuric acid, phosphoric
Z is R4, --NR8 R13, --NR8 --NR13 R14100 H c-Pr 4-CH2SOMe101 H c-Pr 4-CH2SO2from chromium trioxide and aqueous sulphuric acid
R13 is preferably a C1 -C3 alkyl groupl whenacid, hydroiodic acid, sulphuric acid, formic 100° C, in absence of solvents or in a
R12 and R13 are the same or different and nonextreme temperature such as -10°-100° C. nitric acid in the presence of sulphuric acid
Suitable aryl groups R13 are in particular acid, 4-aminonaphthalene-1-sulphonic acid, 5-strength nitrosysulphuric acid are added dropwise
100-associated lipoproteins in a patient comprisingacid, hydrobromic acid, sulphuric acid, phosphoric R13, R14, R15 and R16 are identical or
each R13 is independently a hydrogen atom, an sulphonyl)-ethane-2-ol in 100 parts of ice sulphuric acid half ester by dissolving it in
R1² and R13 have the meanings set forth insulphuric acid, mixtures of trifluoroacetic acid hydroxide (100 ml, 0.100 mol) and water (100
Imidazolyl-substituted phenylpropionic and cinnamic acid derivatives are prepared by reacting appropriate benzyl compounds with imidazoles and optionally vary
##STR44## in which R13 and R14 are acid, hydrobromic acid, sulphuric acid, phosphoricto +100° C., preferably from -10° C. to
solvent at a temperature from 40° to 100° C R10 and R13 to R17 can be linear or branched sulphuric acid, phosphoric acid or nitric acid
R13 =O, H(βOH) or H(β-alkanoyloxy (1-of sulphuric acid or with the Oppenauer method. (10%; 100 ml) was heated on a water bath
(CH2)n --R13, --CH CH--(CH2)n --R13,acid, sulphuric acid, acetic acid, citric acid,100 mg/kg of body weight in 1 to 3 doses
2003519- those where R13 represents a hydroxy group, R14hydrochloric acid, sulphuric acid, organic mono, 100 ° C., preferably -10° to 80° C
R13 represents hydrogen, hydroxyl, methoxy, at temperatures from approximately 0° to 100°acid, sulphuric acid, acetic acid, glycolic acid
560/100, 560/254, 560/255, 562/405, 562/ R13 is hydrogen, lower alkyl, --N(R17, R18 nitric acid and concentrated sulphuric acid
where furthermore one of the radicals R13, R14 for example in the range 70°100° C., for example with 80% strength sulphuric acid,
R11 is OH and R9, R10, R12 and R13 are and Jung (Clinica Chema Acta, 1980, 100, 7-typical of a sulphuric acid ester at 1050 cm-1