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filingDate 1996-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2011-09-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_20cd7fa5546d813c6c8ba89cd0628fd4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8e7e8b53cea6fd2265bed55214e606a1
publicationDate 2011-09-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1186606-B2
titleOfInvention Epothilone derivatives, their preparation and utilization
abstract Epothilone derivatives of formula (I)-(III) are new. R = H or 1-4C alkyl; Y Z = H, halo, pseudohalogen, OH, 1-6C acyloxy, 1-6C alkoxy or benzoyloxy; or Y+Z = bond or O; (a) R' = Q; A = H; B = OR1; and R" = R2; or R"+B = C(O)O, C(S)O, S(O)O, Si(R")2O or C(R")(R"')O; (b) R' = C(=X)Me or CH(OX')Me; A = H; B = OR1; and R" = R2; (c) R' = Q; and A+B = bond; X = O, NOR4, N-NR4R5 or N-NHCONR4R5; X' = H, 1-18C alkyl, 1-18C acyl, benzyl, benzoyl or cinnamoyl; Q = a group of formula (i); and R1-R5 = H, 1-6C alkyl, 1-6C acyl, benzoyl, 1-4C trialkylsilyl, or benzyl or phenyl (both optionally substituted by 1-6C alkoxy, 6C alkyl, OH and halo); or R4+R5 = 2-6C alkylene. Epothilone A and B are excluded. Also claimed is the production of epothilone A or B and/or their 12,13-bis-epi derivatives comprising the epoxidation of epothilone C (for A or derivatives) or D (for B or derivatives) especially using dimethyldioxirane or a peracid.
priorityDate 1995-11-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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