http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-0149070-B1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D205-08
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filingDate 1995-08-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1998-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8b54c600253e9c99dcb27f9f6e324584
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_808da0d6935f1f7c6e0f26ac373beb56
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publicationDate 1998-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-0149070-B1
titleOfInvention Stereoselective preparation of 4-acetoxyazetidinone derivatives
abstract The 4-carboxyzecidinone N-substituent of Structural Formula (I) was electrochemically reacted by applying a direct current to an electrode in the presence of an electrolyte selected from the group consisting of alkali metal salts and amine bases of acetic acid in a mixed solvent of acetic acid and an organic solvent. Then, a method of stereoselectively synthesizing 4-acetoxyazetidinone of formula (II) by one-way reaction by adding only an appropriate amount of water without separating the reaction product and then flowing a direct current under the same conditions to deprotect the aryl group Is provided.n n n n n n n n Wherein R 1 represents a trialkylsilyl group; R 2 represents an aryl group.n n n According to the production method of the present invention, 4-acetoxyazetidinone is obtained in one-way reaction by electrochemical reaction, thus overcoming the problem of environmental stigma with cost reduction; The advantages of easy industrialization, simple manufacturing process and high yield are provided.
priorityDate 1995-08-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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