Patent classifications
C07C45/64
CHROMIUM-FREE HYDROGENATION CATALYST HAVING INCREASED WATER AND ACID STABILITY
The present invention relates to an improved catalyst on the basis of a shaped catalyst body for hydrogenating carbonyl groups in organic compounds under the effect of acids and water, characterized in that the shaped catalyst body contains copper in an amount of 17.5 to 34.5 wt. %, relative to the shaped catalyst body and the copper is present in the shaped catalyst body to at least 70% in the form of a copper spinel CuAl.sub.2O.sub.4. The invention also relates to the production of the catalyst an to the use of same in the hydrogenation of carbonyl groups in organic compounds in the presence of acids and/or water.
Odorous acetals of ethyl vanillin and ethyl vanillin derivatives
The present invention relates to new odorous acetals which are useful as fragrance or flavor materials in particular in providing vanilla and spicy notes with a natural impression resembling vanilla absolute.
Odorous acetals of ethyl vanillin and ethyl vanillin derivatives
The present invention relates to new odorous acetals which are useful as fragrance or flavor materials in particular in providing vanilla and spicy notes with a natural impression resembling vanilla absolute.
Odorous acetals of ethyl vanillin and ethyl vanillin derivatives
The present invention relates to new odorous acetals which are useful as fragrance or flavor materials in particular in providing vanilla and spicy notes with a natural impression resembling vanilla absolute.
SUBSTITUTED HYDROXYSTILBENE COMPOUNDS AND DERIVATIVES SYNTHESIS AND USES THEREOF
The present disclosure relates to substituted hydroxystilbene compounds and derivatives, specifically 2-substituted hydroxystilbene compounds and derivatives, the synthesis of such compounds and their use in therapy.
SUBSTITUTED HYDROXYSTILBENE COMPOUNDS AND DERIVATIVES SYNTHESIS AND USES THEREOF
The present disclosure relates to substituted hydroxystilbene compounds and derivatives, specifically 2-substituted hydroxystilbene compounds and derivatives, the synthesis of such compounds and their use in therapy.
METHOD FOR PRODUCING CYCLIC DIKETONE COMPOUND
Provided is a method for producing a compound represented by general formula (I) by oxidative cleavage of a compound of formula (II), which is a bicyclic tetrasubstituted olefin compound, using hydrogen peroxide. The method for producing a compound represented by general formula (I) includes a step of subjecting a compound represented by general formula (II) to oxidative cleavage using hydrogen peroxide in the presence of an acid catalyst or in the presence of a tungstic acid compound to obtain the compound represented by general formula (I):
##STR00001##
[In the formulae, formula -A.sup.1- (where the front bond denotes a bond that bonds with a carbon atom C.sup.1 while the back bond denotes a bond that bonds with a carbon atom C.sup.2) is an alkylene group having 2 to 6 carbon atoms that may have been substituted and that may further include an ether bond, an ester bond, a secondary amino group, a thioether group, or these, and formula -A.sup.2- (where the front bond denotes a bond that bonds with a carbon atom C.sup.1 while the back bond denotes a bond that bonds with a carbon atom C.sup.2) is an alkylene group having 4 to 10 carbon atoms that may have been substituted and that may further include an ether bond, an ester bond, a secondary amino group, a thioether group, or these.]
METHOD FOR PRODUCING CYCLIC DIKETONE COMPOUND
Provided is a method for producing a compound represented by general formula (I) by oxidative cleavage of a compound of formula (II), which is a bicyclic tetrasubstituted olefin compound, using hydrogen peroxide. The method for producing a compound represented by general formula (I) includes a step of subjecting a compound represented by general formula (II) to oxidative cleavage using hydrogen peroxide in the presence of an acid catalyst or in the presence of a tungstic acid compound to obtain the compound represented by general formula (I):
##STR00001##
[In the formulae, formula -A.sup.1- (where the front bond denotes a bond that bonds with a carbon atom C.sup.1 while the back bond denotes a bond that bonds with a carbon atom C.sup.2) is an alkylene group having 2 to 6 carbon atoms that may have been substituted and that may further include an ether bond, an ester bond, a secondary amino group, a thioether group, or these, and formula -A.sup.2- (where the front bond denotes a bond that bonds with a carbon atom C.sup.1 while the back bond denotes a bond that bonds with a carbon atom C.sup.2) is an alkylene group having 4 to 10 carbon atoms that may have been substituted and that may further include an ether bond, an ester bond, a secondary amino group, a thioether group, or these.]
Metal free process for allylic oxidation
The patent discloses a novel metal free process for the preparation of corresponding phenol and ketone via allylic oxidation of substituted cyclohexenes. Air is used as oxidant in the present process and can be used as such or optionally selected from pure oxygen or atmospheric oxygen. Moreover, the process of the present invention utilizes easily available starting materials and is a green eco-friendly, convenient and economical process with high yield of >60% and high selectivity.
Metal free process for allylic oxidation
The patent discloses a novel metal free process for the preparation of corresponding phenol and ketone via allylic oxidation of substituted cyclohexenes. Air is used as oxidant in the present process and can be used as such or optionally selected from pure oxygen or atmospheric oxygen. Moreover, the process of the present invention utilizes easily available starting materials and is a green eco-friendly, convenient and economical process with high yield of >60% and high selectivity.