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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D317-54
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D317-54
filingDate 1999-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ec5478df739a906d64ad6015d1cb1063
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e5bc52739bb5ba9f97a0d5a7ea14cd98
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f86d479a269b1a92c24369170f52b682
publicationDate 2000-02-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-2340489-A
titleOfInvention 5-(2-Halo-1-hydroxyethyl)-1,3-benzodioxoles and their preparation
abstract The invention relates to a class of enantiomerically pure intermediates represented by Formula I, where X is F, Cl, Br, or I, and a novel enantioselective bioreductive process using yeast to form these intermediates, which are useful in the synthesis of endothelin antagonists, and the like. <EMI ID=1.1 HE=31 WI=46 LX=809 LY=1145 TI=CF>
priorityDate 1998-08-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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