Abstract:
Polytetrahydrofuran ethers of the formulaR.sup.1 --O--(CH.sub.2).sub.4 ].sub.n O--R.sup.2 Iwhere n is a number from 3 to 70, and R.sup.1 and R.sup.2 are hydrocarbon radicals containing 3 to 5 carbon atoms and a double bond, but where R.sup.2 may alternatively be hydrogen.
Abstract translation:式R 1 -O-(CH 2)4] n O-R 2 I的聚四氢呋喃醚,其中n是3-70的数,R1和R2是含有3至5个碳原子和双键的烃基,但R2可以 或者是氢。
Abstract:
The present invention relates to a simplified process, which avoids organo-lithium intermediates, for the preparation of erythro-.alpha.-piperid-2-yl-2,8-bis-(trifluoromethyl)-quinolin-4-yl-methanol, wherein 2,8-bis-(trifluoromethyl)-quinoline-4-carboxylic acid or a salt thereof is reacted with a pyrid-2-yl-magnesium halide to give pyrid-2-yl-2,8-bis-(trifluoromethyl)-quinolin-4-yl ketone in the manner of a Grignard reaction, and this product is hydrogenated, in a conventional manner, to give erythro-.alpha.-piperid-2-yl-2,8-bis-(trifluoromethyl)-quinolin-4-yl-methanol.
Abstract:
The invention relates to special acetals of benzoin compounds which act as photoinitiators, and to a technically simple manufacturing process involving the reaction of an appropriate .alpha.- or .beta.-hydroxyketone with an .alpha.,.beta.-olefinically unsaturated ether in the presence of an acid catalyst. The acetals are particularly suitable for use as photoinitiators in the preparation of photopolymer printing plates.
Abstract:
Reaction products of polymers of C.sub.2 -C.sub.6 -olefins having an average degree of polymerization P of from 5 to 100 and oxides of nitrogen or mixtures of oxides of nitrogen and oxygen are used as additives for fuels, in particular for fuels for gasoline engines.
Abstract:
A process of preparing symmetric C.sub.40 -carotenoids by reacting a C.sub.15 -triphenylphosphonium salt of the formula ##STR1## and a 2,5-bis(1,1-dialkoxy-2-propyl)-2,5-dihydrofuran to form a reaction product containing a diacetyl and a triphenylphosphonium salt, adding a strong base to the reaction product to convert the triphenylphosphonium salt to a carbenium ion, hydrolyzing the diacetyl to a dialdehyde, subjecting the dialdehyde and the carbenium ion to a Wittig reaction to prepare a Wittig reaction product, and converting the Wittig reaction product to the C.sub.40 -carotenoid by acid treatment.
Abstract:
2,5-bis(1,1-dialkoxy-2-propyl)-2,5-dihydrofurans of the formula I ##STR1## where R.sup.1 and R.sup.2 can be identical or different and can be alkyl of 1 to 4 carbons, the preparation thereof by reaction of 2,5-dialkoxy-2,5-dihydrofurans of the formula II ##STR2## In the presence of protic acids or Lewis acids with an alkyl propenyl ether of the formula III ##STR3## and the use thereof for preparing 2,7-dimethyl-2,4,6-octatrienedial and symmetric C.sub.40 -carotenoids such as .beta.-carotene, canthaxanthin and astaxanthin, are described.
Abstract:
Compounds of the formula IR.sup.1 --CH.dbd.CH--R.sup.2 Iwhere R.sup.1 is hydrogen or alkyl and R.sup.2 is alkoxy or acylamino, and R.sup.1 and R.sup.2 together may form a heterocyclic ring, are prepared by elimination of the radical R.sup.3 OH from a compound of the formula II ##STR1## where R.sup.1 and R.sup.2 have the above meanings and R.sup.3 is alkyl, by a method in which the elimination is carried out by passing the compound of the formula II in a liquid or gaseous state into a high-boiling mineral oil above the boiling point of compound I being formed, compound I is taken off in gaseous form, and the high-boiling mineral oil enriched with by-products is removed and replaced with fresh mineral oil.
Abstract:
Polytetrahydrofuran derivatives of the general formula ##STR1## where n is from 2 to 70, X is the bridge member --NH-- or --O-- and R.sup.1 to R.sup.4 are each hydrogen or various radicals.
Abstract:
A process is described for the preparation of cis-2-(1H-1,2,4-triazol-1-ylmethyl)-2-(halophenyl)-3-(halophenyl)oxirane I ##STR1## by epoxidizing Z-3-(1H-1,2,4-triazol-1-yl)-2-(halophenyl)-1-halophenyl)propene II, ##STR2## where halogen is in each case fluorine, chlorine or bromine, which comprises reacting the crude product of the epoxidation with one or more reducing agents, which are added to the reaction mixture in a considerable excess over the amount necessary to destroy any peroxide compounds present.
Abstract:
N-Oxoazolylmethyloxiranes of the formula I ##STR1## where A and B are identical or different and each is alkyl, cycloalkyl, tetrahydropyranyl, benzyl, norbornyl, naphthyl, biphenyl or phenyl, these radicals being unsubstituted or substituted, and X is CH or N, and fungicides and bioregulators containing them.