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filingDate 2002-11-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e201c7dc269302774d33989fc7b0fd69
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_394a00507a7cd58f77661cb950d38af5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2c1579b0a29397aad6b023b0d3d89857
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0edcac8a1fa140f69bc64be703f1fb30
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5de3cb66e26cf96ee6a144e0f103173a
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b0684316a7677595f47b066320a65158
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6281f55472736259486cba224ef250bb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_06b178eb432ea3ca6288c090a9736320
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4247997c9cb20b5d9f1555ae69836cfa
publicationDate 2003-07-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber BG-107301-A
titleOfInvention SYNTHETIC METHOD FOR OBTAINING AN EKETINASCIDINE COMPOUND
abstract The invention relates to processes for the preparation of compounds having a fused ring structure of the formula. These compounds include ecteinascidins and spiroamine-1,4-bridge. The 1,4-bridged method is carried out using a 1-labile, 10-hydroxy, 18-protected hydroxy, di-6,8-ene-5 -one condensed ring compound. After formation of the 1,4-bridge, protection at C-18 is removed prior to spiroamine administration.
priorityDate 1999-05-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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