PubMed:16263102 / 76-337 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/16263102","sourcedb":"PubMed","sourceid":"16263102","source_url":"https://www.ncbi.nlm.nih.gov/pubmed/16263102","text":"5-(1,2,3,4-tetra-O-acetyl-alpha-D-xylopyranos-5S-C-yl)-1,3,4-oxathiazol-2-one (8) has been prepared from glucuronamide in two steps and 73% overall yield by conversion to the tetra-O-acetyl derivative 7 followed by reaction with chlorocarbonylsulfenyl chloride.","tracks":[{"project":"sentences","denotations":[{"id":"TextSentencer_T2","span":{"begin":0,"end":261},"obj":"Sentence"},{"id":"T2","span":{"begin":0,"end":261},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"attributes":[{"subj":"TextSentencer_T2","pred":"source","obj":"sentences"},{"subj":"T2","pred":"source","obj":"sentences"}]},{"project":"NCBITAXON","denotations":[{"id":"T1","span":{"begin":11,"end":18},"obj":"OrganismTaxon"},{"id":"T2","span":{"begin":175,"end":182},"obj":"OrganismTaxon"}],"attributes":[{"id":"A1","pred":"db_id","subj":"T1","obj":"100829"},{"id":"A2","pred":"db_id","subj":"T2","obj":"100829"},{"subj":"T1","pred":"source","obj":"NCBITAXON"},{"subj":"T2","pred":"source","obj":"NCBITAXON"}]}],"config":{"attribute types":[{"pred":"source","value type":"selection","values":[{"id":"sentences","color":"#93ecb0","default":true},{"id":"NCBITAXON","color":"#ec9693"}]}]}}