http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5426228-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C213-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C213-00
filingDate 1994-06-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1995-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_10fa9e53664afdc16bcb08bc8caefd54
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8594660637c0600f4c65c058c1d17d44
publicationDate 1995-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5426228-A
titleOfInvention General method for preparation of sphingosine bases and their analogues
abstract Described herein is a novel method of preparing selectively diastereomers of sphingosine bases and their analogues of general formula (1a) or (1b) ##STR1## where R is an aliphatic or aromatic substituent containing a straight, branched or cyclic chain, which may include one or several heteroatoms as chain members and one or several functional groups as substituents. The method comprises the steps of: n a) converting a starting material into an intermediate product in the form of α,β-unsaturated ketone having the general formula (4a) or (4b) ##STR2## where R is as defined above and PG are any protecting groups compatible with the method, n b) reducing said α,β-unsaturated ketone to an aminoalcohol with DIBAL in toluene to obtain selectively an anti-diastereomer, and n c) removing the protecting groups to obtain the free sphingosine base or its analogue according to formula (1a) or (1b).
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2010085547-A3
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6107520-A
priorityDate 1994-06-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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