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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D341-00
filingDate 2006-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4010a00dfe566266a5d494e6122fc97c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f05b7802a7389be9646928bb19934f20
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_39de011d8263d33145ed2d5293bb7d61
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publicationDate 2008-07-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-101210010-A
titleOfInvention Method for synthesizing macrocyclic polydithioether compound gymnorrhizol
abstract The invention relates to a method for synthesizing novel macrocyclic polydisulfide gymnorrhizol with an active constitutional formula as follows for resisting II-type diabetes. The method comprises: 3, 3'- disulfide group di (2- hydroxy propyl-1- thiosulfate) reacts with 2-hydroxide radical-1, 3- thioglycerin dibasic salt to obtain the gymnorrhizol, or the 3, 3'- disulfide group di (2- hydroxy propyl-1- thiosulfate) reacts with 2-hydroxide radical-1, 3-trimethylene thiosulfate to obtain the gymnorrhizol. The synthetic method of the gymnorrhizol provided by the invention has a new synthetic route, simple operation; compared with the prior art, the method has high yield and good reproduction quality.
priorityDate 2006-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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