(4) ##STR5## wherein R2A is as defined hydrobromic acid, sulfuric acid and phosphoric 100%, based on which 50% inhibition concentration
(3b ): ##STR30## wherein R2a represents a sulfuric acid, phosphoric acid and the like; A mixture of 100 g of benzo[b]thiophen-5-
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R2a, at each occurrence, is selected from H,2002;66(2):93-100; Dolle R E., Mol Diversacids such as hydrochloric, hydrobromic, sulfuric,
R2a, R4a and R6a, which are the same or 100 ng, 4: 50 ng, 5: 10 ng, 6: 5 ngsulfuric acid, and reacting them for 5 to 96
(I): wherein R1, R2a, R2b, R5a, R6a, A, nitric acid, sulfuric acid, sulfonic acid, (such as dioxane) at temperatures between 100 0
acid; a method for clean-up of a contaminated R2A agar medium (Difco), and the plate was 100 ml, into which 20 ml of DPAA5VTE medium
acids, sulfuric acid, hydrochloric acid, in which R1a, R2a and R3 are as defined to about 100° C., frequently under an inert
R1OCONR2a, R1CONR2a, R1S, R1SO, R1SO2, R1 for example sulfuric acid, phosphoric acid or a100 mg/kg of body weight of active compound
2007518- 100, 7971), methodology was developed for acid, boric acid, nitric acid, sulfuric acid, R1A, R2A, R4A and/or R5A are independently
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sulfuric acid, p-toluenesulfonic acid, and the 7 100 183.1 3/4 (35)13 50 204 4/5 (R2a represents a substituted or unsubstituted alkyl
R1, R², R2a, Y and Z are each as acid, sulforous acid, thiosulfuric acid, sulfuric(28.0 ml) was heated at 100°C with stirring
sulfuric, phosphoric, acetic, citric, oxalic, acid to eliminate --OH and --R2a from the 100 mg/kg, preferably from about 5 mg/kg to
R2a, R3a and R4a are are independently selectedacid such as concentrated sulfuric acid and then (100 mg, 0.21 mmole) was dissolved in 2 mL
methyl-N-propylsuccinamic acid, N-(4,5,7-TriR2A is an esterified carboxyl, or an acid 100%, based on which 50% inhibition concentration
where R2a is SO2CF3, SO2CH3, or SO2 (C6 for example sulfuric acid, phosphoric acid or a preferably 0.2 to 100 mg daily or in
R2a and R2b each represents H, a halogen atom(II) with an activated carboxylic acid derivativeFurther elution with System A (100:8:1 ) (
(O)OH and NR2aR2b, wherein R2a and R2b are less than about 100 nm, less than about 50 succinic anhydride or other anhydride or acid
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R2A, or R3A include straight or branched C1-6Under ice cooling, 97% sulfuric acid (1.06 mL,a white, powdery target compound (yield: 100%)
wherein R1a and R2a are independently -H or (3-Methoxyphenyl)butyric acid was dissolved in 30-6-methoxynaphthalene was dissolved in 100 mL of
R2a, R3a, and R4a are independently --H, -acid, such as sulfuric acid, and a suitable 25 ml dimethylformamide was heated at 100° C
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acid esters or amides or cyanoacetic acid esters Xa is --CO--Ya --R2a or --CN, and Xb 100, the sum of m+n+o being at least 3,
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Compound each Y R1 R2a R2b R3 R4 100 H acid, hydroiodic acid, sulfuric acid and or a cholesterol ester transfer protein (CETP)
acid; a method for clean-up of a contaminated R2A agar medium (Difco), and the plate was 100 ml, into which 20 ml of DPAA5VTE medium