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filingDate 2015-06-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-11-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d1d5c7e3843812847115576ee6972bd6
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publicationDate 2021-11-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2873962-T3
titleOfInvention Sulfur (VI) fluoride compounds and methods for their preparation
abstract A compound represented by formula (I): (I) Y-[-Z-(X1-S(O)(X2)F)m]n in which: Y is a biologically active organic central group comprising one or more substituted or unsubstituted moieties selected from an aryl group, a heteroaryl aryl group, a non-aromatic hydrocarbyl group, a non-aromatic heterocyclic group, to which each Z is independently covalently bonded; n is 1, 2, 3, 4 or 5; each Z is independently O, NR or N; when Z is O, m is 1, X1 is a covalent bond and Z is covalently bonded to an aryl or heteroaryl moiety of Y; when Z is NR, m is 1, X1 is a covalent bond or CH2CH2, and Z is covalently bonded to a non-aromatic hydrocarbyl, non-aromatic heterocyclic, aryl, or heteroaryl moiety of Y; when Z is N, (a) m is 2, X1 is CH2CH2 and Z is covalently bonded to a non-aromatic hydrocarbyl, non-aromatic heterocyclic, aryl, or heteroaryl moiety of Y; or (b) m is 1, X1 is a covalent bond or CH2CH2, and Z is a nitrogen on an aromatic or nonaromatic heterocyclic ring portion of the central group Y; each X2 is independently O or NR; and each R independently comprises H or a substituted or unsubstituted group selected from an aryl group, a heteroaryl aryl group, a non-aromatic hydrocarbyl group, and a non-aromatic heterocyclic group.
priorityDate 2014-06-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 75.