http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EA-006369-B1

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filingDate 2001-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5ce80dcfe3034f92341a45e608a1f9d9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2c1579b0a29397aad6b023b0d3d89857
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publicationDate 2005-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EA-006369-B1
titleOfInvention SYNTHETIC METHOD FOR OBTAINING EKTEINASCIDINE COMPOUND
abstract A method for producing compounds with a condensed cyclic structure of the formula (XIV) is described. These products are ecteinascidins, which have a spiroamine-1,4-bridge. This method involves the formation of a 1,4-bridge using a (1-labile) -10-hydroxy- (18-protected hydroxy) di-6,8-en-5-one-fused cyclic compound. After the formation of the 1,4-bridge, the C-18 protection is removed before the introduction of spiroamine.
priorityDate 2000-05-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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