http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5726296-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G03F7-022
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D311-56
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D311-56
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G03F7-022
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D335-06
filingDate 1997-03-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1998-03-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6745f6950f9bbbb7f336b35242308d6a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7433cf19ca48fb73fe2c8bdaa50e1e20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_245a07def58bdc91903d62d6f110cf57
publicationDate 1998-03-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5726296-A
titleOfInvention Process for preparing photoactive coumarin derivatives
abstract Novel processes for the preparation of a new class of coumarin derivatives, which are useful as photoactive compounds in a wide variety of applications including photoresists and other opto-electronic applications, are disclosed and claimed. The process involves a multi-step synthetic method for the preparation of ether, ester, carbonate, or sulfonate derivative of 5-hydroxy, 6-hydroxy, or 7-hydroxy-3-diazo-4-oxo-3,4-dihydrocoumarin starting from the corresponding dihydroxyacetophenone. The compounds formed from the process of the present invention exhibit very high photosensitivity in the deep ultraviolet (DUV) region (ca. 250 nm), and therefore, are useful as photoactive compounds in DUV photoresist formulations.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-0213216-A1
priorityDate 1997-03-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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