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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C35-29
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C45-29
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C29-143
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-433
filingDate 1994-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_79465c1fc7d2039e845c9a6c454394d5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f43f8fba42f73e7e1c4dee039235567d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3a3de1051d8490ce83924d0566c16e8d
publicationDate 1995-11-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H07309795-A
titleOfInvention Process for producing optically active endo-bicyclo [2.2.1 heptan-2-ol
abstract (57) [Summary] [Objective] Optically active endo-bicyclo [2.2.1] heptane-in a high isolation yield using an inexpensive and safe reagent. 2-ol is produced. [Structure] Optically active exo-bicyclo [2.2.1] It is characterized in that heptan-2-ol is oxidized with a sulfonium salt-based oxidant or the like to give optically active bicyclo [2.2.1] heptan-2-one, and further reduced with hydride with diisobutylaluminum hydride or the like. The method for producing optically active endo-bicyclo [2.2.1] heptan-2-ol.
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