http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H1077303-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_62280b798f5d5f885c84e54b3d53ce2f
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08B37-16
filingDate 1996-09-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c3838ec74a7df091ae7e7d3c65b0bff6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_83d6946c21481d8d41d7a5ba1ebf2360
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_441d2fde82cf2e8d4bc96ae762021868
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publicationDate 1998-03-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H1077303-A
titleOfInvention Method for producing cyclodextrin derivative
abstract (57) [Problem] To provide an efficient method for producing a cyclodextrin derivative in which the 2-position hydroxyl group is selectively modified. SOLUTION: A cyclodextrin is reacted with an imidazole derivative represented by the following formula (1) in the presence of molecular sieves to form a 2-position hydroxyl group of at least one D (+)-glucopyranose unit constituting the cyclodextrin. A method for producing a cyclodextrin derivative, comprising obtaining a sulfonylated or acylated cyclodextrin derivative. Embedded image (In the formula, R is an unsubstituted or substituted sulfonyl group, or an unsubstituted or substituted acyl group.)
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2007126494-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107325203-A
priorityDate 1996-09-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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