http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H041163-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_eece3f4c4266dfce4fc469ddcb3eb4e9
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D493-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D317-46
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-23
filingDate 1990-04-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_10bd26b54f5eef5b7262883265336045
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6da9207d734cca5f7d9bf94765f7fd2d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_074f9344e2107b6ad9f638a9432a1a7c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_98665da12d7e262bd2a8e66c72fe6db8
publicationDate 1992-01-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H041163-A
titleOfInvention 3-acetamidochiroinositols and production thereof
abstract NEW MATERIAL:Optically active 1L-3-acetamido-1,4,5,6-tetra-O-acetyl-3-deoxy-2- O-methyl-chiro-inositol shown by formula I. n USE: Useful as a raw material for drugs such as antibiotics and anti-cancer drugs and agricultural chemicals. n PREPARATION: A compound shown by formula I is obtained by a process of subjecting the third position of L-quebrachitol to azide formation, reducing the azide group and acetylating and a process of acetylating hydroxyl groups of the 1, 4, 5 and 6 positions of L-quebrachitol. Optically active 1L-3- acetamido-1,2,4,6-tetra-O-acetyl-3-deoxy-5-O-methyl-chiro-inositol shown by formula II is a new compound and is obtained by a process of subjecting the 4-position of L-quebrachitol to azide formation, reducing the azide group and acetylating and a process of acetylating hydroxyl of the 1, 3, 5 and 6 positions of L- quebrachitol. n COPYRIGHT: (C)1992,JPO&Japio
priorityDate 1990-04-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 23.