| Class / Patent application number | Description | Number of patent applications / Date published |
|---|
| 549399000 |
Chalcogen bonded directly to the hetero ring
| 79 |
| 549408000 |
Chalcogen bonded directly to the carbocyclic ring of the bicyclo ring system (e.g., tocopherols, etc.)
| 25 |
| 549407000 |
Chalcogen or nitrogen attached indirectly to the hetero ring by acyclic nonionic bonding
| 11 |
| 549406000 |
Carbocyclic ring bonded directly to the hetero ring of the bicyclo ring system (e.g., flavanes, etc.)
| 10 |
| 549405000 |
Having -C(=X)-, wherein X is chalcogen, bonded directly to the bicyclo ring system | 4 |
| 20080207928 | Hair and/or Scalp Care Compositions Incorporating Flavonoid Compounds - The invention provides a hair and/or scalp care composition comprising a flavonoid compound of general formula (I) in which: R | 08-28-2008 |
| 20110237808 | METHOD FOR PREPARING NEBIVOLOL - The present invention relates to a process for the preparation of nebivolol and, more particularly, to an improved process of synthesizing an alpha-haloketone of formula | 09-29-2011 |
| 20110251407 | PROCESS FOR PRODUCTION OF OPTICALLY ACTIVE ORGANIC CARBOXYLIC ACID - The present invention is a simple method, in which a specific amount of alkali is added to an enantiomeric mixture of an optically active organic carboxylic acid where enantiomers are present in a non-equimolar ratio, or in which the enantiomeric mixture of an optically active organic carboxylic acid is neutralized with an alkali, and then a specific amount of acid is added thereto, thereby separating an organic carboxylic acid salt in the mother liquor and a crystallized organic carboxylic acid from each other. The method makes it possible to obtain an optically active organic carboxylic acid with improved enantiomeric excess. The present invention provides a simple production method for obtaining an optically active organic carboxylic acid with improved enantiomeric excess from an enantiomeric mixture of an optically active organic carboxylic acid where enantiomers are present in a non-equimolar ratio. | 10-13-2011 |
| 20140005418 | 6-SUBSTITUTED PHENOXYCHROMAN CARBOXYLIC ACID DERIVATIVES | 01-02-2014 |
| 549404000 |
Nitrogen bonded directly to the bicyclo ring system | 2 |
| 20100298580 | Process for the Preparation of 2H-Chromene-3-Carbamate Derivatives - Compounds of formula I, V, VI and II, and processes for their preparation, | 11-25-2010 |
| 20120101287 | Amino-1,3,5-triazines N-substituted with chiral bicyclic radicals, process for their preparation, compositions thereof, and their use as herbicides and plant growth regulators - The invention related to an optically active compound of formula (I) or a salt thereof: | 04-26-2012 |
| Entries |
| Document | Title | Date |
|---|
| 20100010241 | Cosmetics - The present invention provides a cosmetic having equal to or a higher antioxidant activity and moisture retaining property than the above-described conventional vitamin E derivatives. The cosmetic also has an excellent emulsifying ability and solubilizing ability and remarkably reduces a sticky feeling on the skin (in particular, the sticky feeling during drying after the application on the skin). That is, the cosmetic of the present invention containing a vitamin E derivative represented by the following formula (I) or a salt thereof. | 01-14-2010 |
| 20100063305 | METHOD OF PRODUCING S-(-)-6-HYDROXY-2,5,7,8-TETRAMETHYLCHROMANE-2-CARBOXYLIC ACID AND PRODUCT OBTAINED BY THE METHOD - The present invention provides an industrially available method for efficiently producing high-purity S-(−)-6-hydroxy-2,5,7,8-tetramethylchromane-2-carboxylic acid excellent in solid-liquid separability from an S-(−)-6-hydroxy-2,5,7,8-tetramethylchromane-2-carboxylic acid ester, and also provides products obtained by the method. | 03-11-2010 |
| 20100069652 | The Process for Preparing Nebivolol - The present invention relates to a process for the preparation of Nebivolol and, more particularly, to an improved method of synthesizing 6-fluoro chroman epoxides of formula (I) key intermediates in preparing nebivolol. | 03-18-2010 |
| 20110054195 | Synchronized strains of subepidermal cells of muscadine (muscadine sp.) grapevine pericarp for use as a sourse of flavonoids (nutraceuticals) - Methods to generate and isolate novel Synchronized in vitro cell strains of | 03-03-2011 |
| 20120108826 | PROCESS FOR PREPARING NEBIVOLOL - The present invention relates to a process for preparing Nebivolol and, more in particular, to a fractional distillation method of a mixture of stereoisomers of formula | 05-03-2012 |
| 20140155636 | PROCESS OF SEPARATING CHIRAL ISOMERS OF CHROMAN COMPOUNDS AND THEIR DERIVATIVES AND PRECURSORS - The present invention relates to a process of separating chiral isomers of chroman compounds, particularly tocopherols and tocotrienols as well as the esters and intermediates thereof. It has been found that this process allows a separation of the desired isomer with a higher yield and enables the use of the non-desired isomers in a very efficient way. Said process is particularly useful when implemented in an industrial process. Furthermore, it has been found that this process allows using isomer mixtures as they result from traditional industrial synthesis. | 06-05-2014 |
| 20160017150 | METHOD OF ISOLATING BLUE ANTHOCYANIN FRACTIONS - The present invention is directed to a method of isolating fractions of anthocyanin molecules from anthocyanin-containing vegetable and fruit juices and extracts, or combinations thereof, at a select pH based on differences in polarity of the anthocyanin molecules in the anthocyanin-containing vegetable and fruit juices and extracts. | 01-21-2016 |
