http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H06322001-A

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filingDate 1993-05-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8f28ccf5df4c7aa1205fdd60ab98f43a
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publicationDate 1994-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H06322001-A
titleOfInvention New substances, their manufacturing methods and uses
abstract (57) [Summary] [Structure] The amylose derivative is chemically bonded to the inner and outer surfaces of the pores of the porous carrier through a cross-linking agent at a part of the hydroxyl group at the 6-position of amylose, and is represented by the following general formula (1). Substances whose main structure is the following structure: After protecting part or all of the hydroxyl group at the 6-position of amylose with a protecting group and introducing a substituent into the remaining hydroxyl group, A method for producing the above novel substance, characterized in that the protecting group is removed, and a part of the hydroxyl group at the 6-position is chemically bonded to the inner and outer surfaces of the pores of the porous carrier through a cross-linking agent, and for chromatography containing the new substance. Separation agent. According to the present invention, an amylose derivative in which a specific substituent is introduced into a part or all of hydroxyl groups is It is possible to efficiently obtain a novel substance chemically bonded to the porous carrier through the crosslinking agent at the hydroxyl group at the position. This material is useful as a chromatographic packing material for optical resolution.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7399409-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2013088398-A
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2003530969-A
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priorityDate 1993-05-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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