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公开(公告)号:DK162280B
公开(公告)日:1991-10-07
申请号:DK665474
申请日:1974-12-19
Applicant: BASF AG
Inventor: HOFFMANN WERNER , HIMMELE WALTER , PAUST JOACHIM , FRAUNBERG KARL VON , SIEGEL HARDO , PFOHL SIGBERG
IPC: C07C31/137 , C07B61/00 , C07C27/00 , C07C29/14 , C07C29/141 , C07C41/00 , C07C43/303 , C07C45/00 , C07C45/50 , C07C47/347 , C07C47/45 , C07C51/00 , C07C61/13 , C07C67/00 , C07C69/753 , C07C209/00 , C07C209/26 , C07C209/28 , C07C209/52 , C07C209/88 , C07C211/03 , C07C211/17 , C07C211/19 , C07C211/27 , C07C211/38 , C07C211/44 , C07C213/08 , C07C231/00 , C07C231/02 , C07C233/55 , C07D295/02 , C07D295/03 , C07D295/22
Abstract: Pinanes substituted by a group X in the 3-position which group is formyl, or its alkyl-acetals or alkyl-hemiacetals, carboxylic acid, carboxylic acid chloride, carboxylic acid amide, hydroxymethyl or aminomethyl substituted in a specific manner at the nitrogen, the optical isomers of these compounds and a process for their manufacture by hydroformylation of alpha -pinene in the presence of rhodium catalysts, and conversion of the 3-formylpinane first produced into the above derivatives by conventional methods.
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公开(公告)号:DK433689A
公开(公告)日:1990-03-03
申请号:DK433689
申请日:1989-09-01
Applicant: BASF AG
Inventor: PAUST JOACHIM , ERNST HANSGEORG
IPC: C07D239/42
Abstract: In an improved process for the preparation of 2-n-propyl-4-amino-5-methoxymethyl-pyrimidine of the formula I I by reacting butyramidine II II with alpha -methoxymethyl- beta -methoxyacrylonitrile III III the butyramidine II is reacted with a 0.4-5 molar excess of alpha -methoxymethyl- beta -methoxyacrylonitrile III at from -10 DEG to +20 DEG C.
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公开(公告)号:CA1262910A
公开(公告)日:1989-11-14
申请号:CA497801
申请日:1985-12-17
Applicant: BASF AG
Inventor: WUEST HANS-HEINER , FRICKEL FRITZ-FRIEDER , PAUST JOACHIM , SCHMIEDER KLAUS , NUERRENBACH AXEL
IPC: C07C63/04 , C07D257/04 , C07C175/00 , A61K31/00
Abstract: Substituted hexatriene derivatives of the formula (I): (I) where R1 is methyl, nitrile, C2-C10-ketal, tetrazolyl, -CH2OR2, -CH2NR3R4 or -COR5, where R2 is hydrogen, C1-4-alkyl, C1-20-alkanoyl or unsubstituted benzoyl or benzoyl substituted by methyl, methoxy, halogen or nitro, R3 and R4 are hydrogen, C1-6-alkanoyl or unsubstituted benzoyl or benzoyl substituted by methyl, methoxy, halogen or nitro, and R5 is hydrogen, C1-4-alkyl, halogen, -OR6 or -NR7R8, where R6 is hydrogen, unsubstituted or hydroxyl-substituted C1-6-alkyl, phenyl or aralkyl, and R7 and R8 are hydrogen, unsubstituted or hydroxyl-substituted C1-6-alkyl, phenyl or aralkyl, and, where relevant, their physiologically tolerated salts are descrobed, together with a process for their preparation. These compounds are useful in the topical and systemic therapy of acne, psoriasis and other dermatological disorders associated with pathologically modified keratinization. They may also be used for topical and systemic therapy, and for prophylaxis, of precanceroses and carcinomas of the skin, the mucous membranes and internal organs, as well as for the treatment of rheumatic disorders, especially disorders of an inflammatory or degenerative nature which affect the joints, muscles, sinews and other parts of the locomotor apparatus.
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公开(公告)号:DK155044B
公开(公告)日:1989-01-30
申请号:DK351976
申请日:1976-08-04
Applicant: BASF AG
Inventor: PAUST JOACHIM , SCHNEIDER JOACHIM , JAEDICKE HAGEN
IPC: C07B61/00 , B01J21/00 , B01J23/00 , C07C20060101 , C07C49/21 , C07C49/653 , C07C67/00 , C07C67/30 , C07C69/52 , C07C401/00 , C07C403/00 , C07C403/24
Abstract: Process for the manufacture of canthaxanthin by oxidizing beta -carotene, retro-dehydro-carotene or echinenone with a salt of chloric or bromic acid in the presence of a catalyst and of an inert diluent or solvent.
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公开(公告)号:DK10886A
公开(公告)日:1986-08-16
申请号:DK10886
申请日:1986-01-10
Applicant: BASF AG
Inventor: PFAFF KLAUS-PETER , PAUST JOACHIM , HARTMANN HORST
Abstract: Sugar ketals are prepared by reacting a sugar with a ketone in the presence of an acid catalyst by a process in which A. a molecular boron trifluoride compound or trifluoromethanesulfonic acid is used in an amount of only from 0.01 to 10% by weight, based on the sugar used, B. up to a 30-fold molar excess of the ketone is used and C. the water formed during the reaction is removed continuously from the reaction mixture. In a particularly advantageous embodiment of the process, the boron trifluoride is used in the form of boron trifluoride etherate and, when the reaction is complete, this compound or the trifluoromethanesulfonic acid is rendered ineffective under non-aqueous conditions, after which the ketone is evaporated off and the reaction mixture is then subjected to fractional distillation. The process is particularly important for the reaction of L-sorbose with acetone to obtain 2,3:4,6-di-O-isopropylidene-L-sorbofuranose, which is required for the synthesis of ascorbic acid.
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公开(公告)号:CA1204120A
公开(公告)日:1986-05-06
申请号:CA431302
申请日:1983-06-28
Applicant: BASF AG
Inventor: VOGEL FRIEDRICH , PAUST JOACHIM , NUERRENBACH AXEL
Abstract: The present invention relates to a compound having the general formula (II) (II) in all its isomeric forms, in which Z is selected from the group consisting of wherein R2 is alkyl of 1 to 4 carbon atoms, and the dotted line indicates that the compound may have an additional double bond. These compounds can be used to make intermediate compounds having the general formula I (I) in which R1 is H, an alkyl, arylalkyl or an aliphatic acyl radical; X and Y together provide an additional bond or Y is OH and X is H; and in which the dotted line can represent an additional bond. The compounds of general formula (I) can in turn be used to make .alpha.-tocopherol or a 6-0-derivative thereof.
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公开(公告)号:DK527283D0
公开(公告)日:1983-11-17
申请号:DK527283
申请日:1983-11-17
Applicant: BASF AG
Inventor: PAUST JOACHIM , LEININGER HARTMUT
IPC: C07D307/33 , C07D307/60 , C07D307
Abstract: Dihydro-4,4-dimethylfuran-2,3-dione is prepared by oxidation of racemic dihydro-3-hydroxy-4,4-dimethyl-2(3H)-furanone by a process in which the oxidation is carried out by gradually adding powdered calcium oxide to a solution of racemic dihydro-3-hydroxy-4,4-dimethyl-2(3H)-furanone and chlorine in the inert organic solvent.
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公开(公告)号:CA1151658A
公开(公告)日:1983-08-09
申请号:CA349380
申请日:1980-04-08
Applicant: BASF AG
Inventor: JAEDICKE HAGEN , PAUST JOACHIM
IPC: C07D319/06 , C07D317/06
Abstract: A process for the preparation of 6-membered cyclic acetals of trans-4-chloro-3-methyl-but-2-en-1-al by reacting the corresponding acetals of 3-methyl-but-2-en-1-al (prenal), in a halohydrocarbon, with sulfuryl chloride and for their subsequent oxidate on to trans-3-methyl-but-2-ene-1,4-di-al-1-monoacetals (3-methyl-fumarodialdehyde-1-mono-acetals), The trans-3-methyl-but-2-ene-1,4-dial-1-monoacetals are of great importance in terpene syntheses, since they make it possible to carry out successive Wittig reactions giving a very large number of compounts of biological and pharmacological importance.
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公开(公告)号:CA1127170A
公开(公告)日:1982-07-06
申请号:CA336670
申请日:1979-09-28
Applicant: BASF AG
Inventor: PAUST JOACHIM , NUERRENBACH AXEL
IPC: A61K31/195 , A61K31/07 , A61K31/16 , A61K31/165 , A61K31/20 , A61P17/00 , A61P35/00 , C07C67/00 , C07C401/00 , C07C403/00 , C07C403/20 , C07C175/00
Abstract: O.Z. 0050/033446 of the disclosure: all-E- and 13-Z-retinic acid compounds of the formulae I and II II where the broken line is a chemical bond or two hydrogen atoms and the carboxyl group in the aromatic ring may be in the ortho-, meta- or para-position, the preparation of these compounds, pharmaceutical formulations containing these compounds, and their use as drugs in the topical and systemic therapy and prophylaxis of precancerous conditions and carcinomas, and of dermatological disorders
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公开(公告)号:CA1080243A
公开(公告)日:1980-06-24
申请号:CA292829
申请日:1977-12-09
Applicant: BASF AG
Inventor: JAEDICKE HAGEN , PAUST JOACHIM , SCHNEIDER JOACHIM U
IPC: C09B61/00 , C07C20060101 , C07C67/00 , C07C401/00 , C07C403/00 , C07C403/24 , C07G20060101 , C07C175/00
Abstract: A process for the manufacture of canthaxanthin by oxidizing isozeaxanthin or 4'-hydroxyechinenone with a salt of chloric acid or of bromic acid in the presence of a catalyst and of an inert diluent or solvent at from 0 to 100.degree.C. Suitable catalysts are the halogens bromine and iodine.
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