http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-0023414-A3

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ebb6a553affdc364c91cffe3baf12564
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07B2200-07
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C2601-14
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C68-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C67-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C69-96
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C213-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C219-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C51-487
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C229-36
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-732
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-487
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B57-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C219-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-96
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C59-11
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C59-54
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C213-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C229-36
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-43
filingDate 1999-10-22^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f33ad384b15c2e94dff3348f2c44d55a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cc8612094babedbdd74ce41b99cb7c9d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_32b03c51acb5c08b6abf85195c78266d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6ccb4031d1c207b52bed79ce8396a032
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_afe2cc515dd5ddc068f662151589ccc8
publicationDate 2001-12-13^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-0023414-A3
titleOfInvention Synthesis of optically active cyclohexylphenylglycolic acid and its esters
abstract A process for the preparation of optically active cyclohexylglycolate esters is described. The process utilizes carboxylic acid activation to couple (R)- or (S)-cyclohexylphenylglycolic acid (CHPGA) with 4-N,N-diethylamino butynol or other propargyl alcohol derivatives. The preparation of the hydrochloride salt is also described. In addition, a resolution process employing tyrosine methyl ester enantiomers for preparing a single enantiomer of CHPGA from racemic CHPGA is disclosed.
priorityDate 1998-10-22^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226653600
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226556237
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226556416
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID777375
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID231489435
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID76957
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226556238
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22013162
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226652016
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID53407507
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID97700
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID70652

Showing number of triples: 1 to 45 of 45.