http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20040097706-A

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J2531-822
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F7-0812
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-2208
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-10
filingDate 2003-05-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b23d087707f3519b3f3d6625ffb3c36d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_878fe1dfd8308300c9a326129c0808dd
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publicationDate 2004-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20040097706-A
titleOfInvention Compounds of cis-2-alkenyl-trialkylsilyl substituted 5 or 6-membered cycloalkanol and the manufacturing method thereof
abstract The present invention is carried out a carbonylation reaction of an allenylaldehyde or a ketone of the formula (2) with a trialkylsilylhydride of the formula (3) and a rhodium catalyst under carbon monoxide to give various cis stereoselective compounds of the formula (1) An alkenyl-trialkylsilyl-substituted 5 or 6-cyclo alkanol compound. The compound of formula (1) produced according to the preparation method of the present invention is a compound useful for the preparation of natural products and bioactive substances, and is a novel intermediate provided by the present invention.n n n n n n n n n n (1) (2) (3)n n n [Wherein, X is any one of tosyl amine, oxygen, malonic acid ester, R 1 is either hydrogen, lower alkyl, phenyl, R 2 is a C 1 to C 10 alkyl group or phenyl group, n is Number 1 or 2.]
priorityDate 2003-05-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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