Zobrazeno 1 - 10
of 116
pro vyhledávání: '"Laurean, Ilies"'
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-8 (2024)
Abstract Exploitation of noncovalent interactions for recognition of an organic substrate has received much attention for the design of metal catalysts in organic synthesis. The CH–π interaction is especially of interest for molecular recognition
Externí odkaz:
https://doaj.org/article/11147beb830e49a1af66f307d33e67f6
Publikováno v:
Communications Chemistry, Vol 4, Iss 1, Pp 1-8 (2021)
Halogen–sodium exchange reactions with neopentyl sodium provides access to a range of aryl and alkenyl organosodium compounds in situ, as an alternative to organolithium reagents.
Externí odkaz:
https://doaj.org/article/626699ad3e384132a0b589a7bde5ecbe
Autor:
Olena Kuleshova, Laurean Ilies
Publikováno v:
Transition‐Metal‐Catalyzed C‐H Functionalization of Heterocycles. :609-630
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c49c386d091c4cbbde4566b4a635c465
https://doi.org/10.1002/9781119774167.ch14
https://doi.org/10.1002/9781119774167.ch14
Autor:
Sobi Asako, Laurean Ilies
Publikováno v:
Handbook of CH-Functionalization. :1-15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c5ee6af60f1d8268dd4cca685c9db28
https://doi.org/10.1002/9783527834242.chf0137
https://doi.org/10.1002/9783527834242.chf0137
Publikováno v:
Science. 375:658-663
Regioselective functionalization of arenes remains a challenging problem in organic synthesis. Steric interactions are often used to block sites adjacent to a given substituent, but they do not distinguish the remaining remote sites. We report a stra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4867c921f4ec4bc527e9a0b0bc49ea1
https://doi.org/10.1126/science.abm7599
https://doi.org/10.1126/science.abm7599
Publikováno v:
Synlett.
2,2′-Bipyridine derivatives were synthesized by dehydrogenative dimerization of nonactivated pyridines using sodium dispersion. The reaction features operational simplicity, mild conditions, and the use of earth abundant and nontoxic sodium as the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56c2da650619b1c7fd9317ca17e3b5f4
https://doi.org/10.1055/a-2047-8355
https://doi.org/10.1055/a-2047-8355
Publikováno v:
Nature Catalysis. 4:631-638
Regioselective thienyl–thienyl coupling is arguably one of the most important transformations for organic electronic materials. A prototype of ideal organic synthesis to couple two thienyl groups by cutting two C–H bonds requires formal removal o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc7f63b8f445d2c823dc3430f40f0758
https://doi.org/10.1038/s41929-021-00653-7
https://doi.org/10.1038/s41929-021-00653-7
Publikováno v:
Chemistry Letters. 51:38-40
An easy-to-handle sodium dispersion in paraffin oil (SD), in combination with inexpensive and environmentally benign 1,3-dimethyl-2-imidazolidinone (DMI) as an additive enables the Birch-type reduc...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cbc16cb64acb4f00bd88a45d3498c62d
https://doi.org/10.1246/cl.210546
https://doi.org/10.1246/cl.210546
Publikováno v:
Organic letters. 24(39)
A catalytic amount of Mo(CO)6 and an ortho-quinone ligand, in the presence of triphenylphosphine as a mild reductant enables the intermolecular reductive coupling of aromatic aldehydes and the intramolecular cou-pling of aromatic ketones to produce f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bdfe709bc09f6a976b4b8eff1b5b1c1
https://pubmed.ncbi.nlm.nih.gov/36166349
https://pubmed.ncbi.nlm.nih.gov/36166349
Publikováno v:
ACS Catalysis. 11:5968-5973
A terpyridine derivative and an iridium complex catalyze the C–H borylation of a stoichiometric amount of a fluoroarene with high ortho-selectivity and tolerance of functional groups such as bromid...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b67308765f812bb29f63a70a1504d069
https://doi.org/10.1021/acscatal.1c01206
https://doi.org/10.1021/acscatal.1c01206