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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D257-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P43-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-41
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D257-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P43-00
filingDate 1991-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0ec3215fd80308ef6c59e352aeaa5e1a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cfe1f89342193fd2f6aeed955d2bc10d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8850a3e9e774931613dd778cb31d21e3
publicationDate 1991-11-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0455423-A2
titleOfInvention Ortho-lithiation process for the synthesis of 2-substituted 1-(tetrazol-5-yl) benzenes
abstract A process utilizes the tetrazole functional group to direct lithiation at the ortho position of a phenyltetrazole and generate a nucleophilic aryllithium species which then undergoes reaction with an electrophile to generate a 2-substituted 1-(tetrazol-5-yl)benzene. The process is useful in the production of intermediates in the synthesis of angiotensin II antagonists. This novel process is a more cost effective and versatile route for the large-scale preparation of these key intermediates.
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0643704-A1
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0540356-A2
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5965738-A
priorityDate 1990-05-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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