http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9790192-B2

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D341-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D495-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D251-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C321-16
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D341-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D251-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D495-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C321-16
filingDate 2015-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2017-10-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e7841bd36619e1dc0319997cb1a246cc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_58f6e4841f7eed434e34db47e2f8fe90
publicationDate 2017-10-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-9790192-B2
titleOfInvention Synthesis of cyclophanes from a self-assembly reaction
abstract Disclosed herein is a novel method for preparing cyclophanes, comprising forming a disulfide cyclophane by contacting a linker moiety which includes two or more thiol groups, with a metal salt and an oxidant. The disulfide cyclophane is then desulfurized to form a thiacyclophane comprising thioether bridges. This thiacyclophane optionally may be further desulfurized to form an unsaturated hydrocarbon cyclophane, which can then be reduced to form a saturated hydrocarbon cyclophane. The various cyclophanes can be synthesized in a ring form, such as a dimer, trimer or tetramer etc., or they can be synthesized in a tetrahedral or larger structure. Also disclosed are novel cyclophanes formed by the disclosed method.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-10344005-B2
priorityDate 2014-11-18-04:00^^<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: 499.