Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Li-Qiu Liu"'
Publikováno v:
Results in Chemistry, Vol 3, Iss , Pp 100220- (2021)
A rapid and efficient NFSI-mediated hydroxy or alkoxy-selenation of internal alkenes and chalcones is presented. This reaction proceeds smoothly at room temperature and features broad substrate scope, which employs NFSI as the oxidizing agent, afford
Externí odkaz:
https://doaj.org/article/38d48058f94749d1b0e95d1e5dd8eabc
Publikováno v:
The Journal of Organic Chemistry. 87:15120-15128
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fac3db3ce0e2f43887904b780c270ea0
https://doi.org/10.1021/acs.joc.2c01622
https://doi.org/10.1021/acs.joc.2c01622
Publikováno v:
The Journal of Organic Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc4b93d8f55181409c9c9bfbe452195b
https://doi.org/10.1021/acs.joc.2c01969
https://doi.org/10.1021/acs.joc.2c01969
Publikováno v:
Organic & Biomolecular Chemistry. 18:655-659
We developed an efficient and novel protocol to synthesize 2-alkynyl oxazoles from tert-butyl isocyanide and alkynyl carboxylic acids. This method allowed the synthesis of diversely functionalized oxazoles under mild reaction conditions, coupled with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f53a002dbf3ac024da04a39f45ab13be
https://doi.org/10.1039/c9ob02337b
https://doi.org/10.1039/c9ob02337b
Publikováno v:
Organic & Biomolecular Chemistry. 18:8089-8093
A novel and efficient one-pot synthesis of symmetrical N-aryl dialkynylimines via palladium-catalyzed and copper-promoted isocyanide insertion, cross-coupling and elimination has been developed. This method features readily available starting materia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bbaac88ddd7a510bb11a7ee223908c98
https://doi.org/10.1039/d0ob01604g
https://doi.org/10.1039/d0ob01604g
Publikováno v:
Energy Economics. 83:333-344
China's electric power industry has experienced a reform whereby the generation sector is being opened up to competition but the transmission and distribution sectors are still under regulation. Efficiency and benchmarking analyses are widely used fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b80d90467877bd85639e744e27cfcea9
https://doi.org/10.1016/j.eneco.2019.07.001
https://doi.org/10.1016/j.eneco.2019.07.001
Publikováno v:
Advanced Synthesis & Catalysis. 361:1887-1895
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::39bc608cfef383f65062a1cd1e67c9ff
https://doi.org/10.1002/adsc.201801245
https://doi.org/10.1002/adsc.201801245
Publikováno v:
Organicbiomolecular chemistry. 18(40)
A novel and efficient one-pot synthesis of symmetrical N-aryl dialkynylimines via palladium-catalyzed and copper-promoted isocyanide insertion, cross-coupling and elimination has been developed. This method features readily available starting materia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d0e9806f3f2a2ebe12bbb93f99b7a714
https://pubmed.ncbi.nlm.nih.gov/33026017
https://pubmed.ncbi.nlm.nih.gov/33026017
Publikováno v:
Journal of Energy Engineering. 146
China’s thermal power generation has attracted worldwide attention because of its significantly high amount of carbon emissions and environmental protection measures. The focus of efficienc...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32c50344310023e5efba26b40c009807
https://doi.org/10.1061/(asce)ey.1943-7897.0000678
https://doi.org/10.1061/(asce)ey.1943-7897.0000678
Publikováno v:
Organicbiomolecular chemistry. 18(4)
We developed an efficient and novel protocol to synthesize 2-alkynyl oxazoles from tert-butyl isocyanide and alkynyl carboxylic acids. This method allowed the synthesis of diversely functionalized oxazoles under mild reaction conditions, coupled with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d688d11c055416bdb8e66b951ef5ce2e
https://pubmed.ncbi.nlm.nih.gov/31930236
https://pubmed.ncbi.nlm.nih.gov/31930236