http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2008064886-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1506cbf417bfdd87c7ce6fc50c480653
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-92
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-92
filingDate 2005-07-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b2e8a43bbc9c5df62c704b38cb194664
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_32327a27d748ef56c59d68e000b5aee3
publicationDate 2008-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2008064886-A1
titleOfInvention Process for the Preparation of Optically-Active Compounds
abstract A method of preparing enatiomerically enriched 3a,6,6,9a-tetramethyl-dodecahydro-naphtho[2,1-b]furan, formula (I), from (E,E)-homofarnesic acid or (E)-monocyclohomofarnesic acid by (a) reacting firstly with a chiral alcohol, (b) reacting the product of (a) with an acid to cause a first cyclisation, (c) producing an alcohol by reacting the product of (b) with a reducing agent and (d) causing a second cyclisation by reacting the product of (c) with an acid. The product of this process gives a mixture of both enantiomers with one in excess.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8765980-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10081613-B2
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9732056-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8933253-B2
priorityDate 2004-07-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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