Predicate |
Object |
assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_087bed7abab91ae0f927879f9fe8b273 |
classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J2540-62 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J2540-34 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J2540-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J2540-225 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J2540-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J2531-821 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J2540-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J2231-543 |
classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-181 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D313-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08F132-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-1825 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-2208 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-2291 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-2278 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-226 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-2273 |
classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D313-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-22 |
filingDate |
2018-04-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate |
2021-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d1b2c7748aa6e80d7cabf4c285c39893 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_560f9cd65c24448b898bf0af6ebeabe3 |
publicationDate |
2021-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber |
US-11053209-B2 |
titleOfInvention |
Highly efficient synthesis of z-macrocycles using stereoretentive, ruthenium-based metathesis catalysts |
abstract |
A highly efficient, Z-selective ring-closing metathesis system for the formation of macrocycles using a stereoretentive, ruthenium-based catalyst supported by a dithiolate ligand is reported. This catalyst is demonstrated to be remarkably active as observed in initiation experiments showing complete catalyst initiation at −20° C. within 10 min. Using easily accessible diene starting materials bearing a Z-olefin moiety, macrocyclization reactions generated products with significantly higher Z-selectivity in appreciably shorter reaction times, in higher yield, and with much lower catalyst loadings than in previously reported systems. Macrocyclic lactones ranging in size from twelve-membered to seventeen-membered rings are synthesized in moderate to high yields (68-79% yield) with excellent Z-selectivity (95%-99% Z). |
priorityDate |
2017-05-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type |
http://data.epo.org/linked-data/def/patent/Publication |