http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2421206-A1

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C309-63
filingDate 2001-09-18^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_656c0b5202442bc238f80cc5afc4989f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_47da9bc514fceac0d8580fe3c860d169
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publicationDate 2002-03-28^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2421206-A1
titleOfInvention Oxime derivatives and the use thereof as latent acids
abstract New oxime sulfonate compounds of formula (I, II, III, IV, V, VI and VII) wherein R1 is for example C1-C18 alkylsulfonyl, R2 is halogen or C1-C10 haloalkyl; R3 is for example unsubstituted or substituted phenylenedisulfonyl, diphenylenedisulfonyl, or oxydiphenylenedisulfonyl; Ar1 is for example a direct bond, C1-C12 alkylene; -O-C-bond or a O-Si-bond which cleaves upon the action of an acid; A1, A2, A3, A4, A5, A6, A7, A8, A9, A10, A11 and A12 are for example a direct bond, -O-, or S-, or are C1-C12 alkylene or phenylene unsubstituted or substituted; Y1 is C1-C12 alkylene which is for example subsituted by OR4, or SR7; Y2 is e.g. a trivalent radical of C1-C12 alkylene; Y3 is e.g. a tetravalent radical of C1-C12 alkylene; X is halogen; Ar'1 is for example C1-C12 alkyl which is unsubstituted or substituted; Ar"1 is for example phenylene; provided that at least one of the radicals Ar'1, Ar"1, is substituted by 1 to 3 groups of (VIII), (IX), (X), (XI), (XII) and/or (XIII); M+ is e.g. (XIV); L- is for example halogen; R15, R16, R17 and R18 are e.g. hydrogen or phenyl; R19, R20, R21, R22 and R23 are e.g. phenyl; are especially suitable for the preparation of photoresists.
priorityDate 2000-09-25^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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