http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H04154775-A

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-33
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D315-00
filingDate 1990-11-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a67f04683b8f91bebac7293f7877c0d8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8026cce86f9bac03ad68efd440fa326a
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publicationDate 1992-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H04154775-A
titleOfInvention Production on trans-3,4-disubstituted gamma-lactone compounds
abstract PURPOSE: To obtain trans-3,4-disubstituted γ-lactone compounds having a high optical purity in simple steps by using levoglucosenone as a starting substance and forming a lactone ring using the Baeyer-Villiger oxidative reaction. n CONSTITUTION: An alkyl group R 1 (R 1 is alkyl or alkenyl) is added to an enone part of levoglucosenone expressed by formula I that is a thermal decomposition product of cellulose to provide a compound expressed by formula II, which is then subjected to the Baeyer-Villiger oxidation using a peracid (e.g. peracetic acid). Thereby, a lactone ring is formed to afford a compound expressed by formula III. The OH of the resultant compound expressed by formula III is subsequently converted into a leaving group OR 2 to provide a compound expressed by formula IV. Alkylation or alkenylation is then carried out in the presence of a copper salt (e.g. copper iodide) to afford a compound expressed by formula V, which is an aromatic ingredient in whiskies, etc., and utilized as a pheromone in the insect kingdom. n COPYRIGHT: (C)1992,JPO&Japio
priorityDate 1990-05-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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