摘要:
Substituted 2,3-dihydrobenzofurylmethyl esters of the formula I ##STR1## where R.sup.8 is hydrogen or alkyl of up to 5 carbon atoms, R.sup.9 is alkyl, haloalkenyl or haloalkynyl, each of up to 5 carbon atoms,R.sup.10 is halogen or alkyl of up to 5 carbon atoms,R.sup.11 is halogen or alkyl of up to 5 carbon atoms, A is halogen, alkyl, alkoxy, trihaloalkyl or trihaloalkoxy, each of up to 5 carbon atoms, cyano or nitro,B is alkyl, alkenyl or alkynyl, each of up to 4 carbon atoms, or an alicyclic radical of 3 to 7 carbon atoms and n is from 0 to 3,R.sup.2 is hydrogen, cyano or alkyl, alkenyl or alkynyl, each of up to 5 carbon atoms, andR.sup.3, R.sup.4, R.sup.5, R.sup.6 and R.sup.7 are identical or different and each is hydrogen, halogen or alkyl, alkenyl, alkynyl or alkoxy, each of up to 5 carbon atoms, and R.sup.9 may also be alkenyl of up to 5 carbon atoms if R.sup.2 is cyano or is alkyl, alkenyl or alkynyl, each of up to 5 carbon atoms.The novel compounds are useful in pest control.
摘要:
New pyridinyl aminoalkyl ethers, their N-oxides and their physiologically acceptable addition salts with acids, processes for their preparation and pharmaceutical formulations which contain these compounds and are useful in the treatment of cardiac arrhythmias.
摘要:
Chirally substituted 2-imidazolin-5-ones and their use as intermediates for the preparation of optically active aminoacids, especially of optically active .alpha.-substituted aminoacids.
摘要:
4-.alpha.-Amino-arylmethyl-6-methyl-1,3-dihydro-furo[3,4-c]pyridin-7-ols of the formula ##STR1## where R.sup.1 and R.sup.2 together are alkylene which may be interrupted by a hetero-atom and may be substituted by C.sub.1-4 -alkyl, andR.sup.3 and R.sup.4 are hydrogen, hydroxyl, C.sub.1-3 -alkyl, C.sub.1-3 -alkoxy or halogen,processes for their preparation, and their use for the preparation of pyridinyl aminoalkyl ethers.
摘要:
An industrially advantageous process for the manufacture of vitamin B6 (pyridoxin) from 2-methyl-3-hydroxy-4,5-bis-(halomethyl)-pyridine, wherein the starting compound is first converted in the conventional manner to the corresponding pure acetoxy compound which is reacted with an alkali metal acetate, alkaline earth metal acetate or tertiary ammonium acetate to give pyridoxin triacetate, from which pyridoxin can be liberated by hydrolysis or trans-esterification.
摘要:
New pyridin-3-ols and their N-oxides and acid addition salts, which are useful as intermediates, especially for the preparation of pharmacologically active compounds, and their preparation.
摘要:
4-Methyloxazole is manufactured by reaction of formimido-esters with hydroxyacetone. 4-Methyloxazole, manufactured by the process of the invention, is a starting material for the manufacture of dyes, pharmaceuticals, pesticides and vitamins.
摘要:
A process for the manufacture of .beta.-bromoalkylsulfones and .beta.-bromoalkenylsulfones by addition reaction of sulfonic acid bromides with olefins or acetylenes in the presence of hydroperoxide and, optionally, of metal salts. Starting materials for further syntheses and for biologically active compounds may be obtained by subsequent dehydrobromination of the addition products.