http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2240413-C

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_843896afb26488b322226f1eb90ae02d
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H1-00
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H1-00
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filingDate 1996-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2008-09-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_00459e528dda1dac2a531af7f4ffaff2
publicationDate 2008-09-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2240413-C
titleOfInvention Selective alkylations of cyclodextrins at the levels of minimal effective basicity
abstract By controlling basicity of the reaction, it is possible to alkylate preferentially the secondary hydroxyls of cyclodextrins. These hydroxyls surround the principal, wide, entry into the cyclodextrin cavity and, thus, their substitution by suitably chosen substituents can improve the formation of inclusion complexes. By methods of the invention, cyclodextrin derivatives substituted with fused 1,4-dioxane ring(s) can be obtained. If a reagent with one alkylating moiety is used, a mixture of ethers of cyclodextrin is formed. Using methods of this invention, up to 96 % of the substitution can be directed to the secondary hydroxyls.
priorityDate 1995-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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