Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Hoimin, Jung"'
Autor:
Hoimin Jung1,2, Jeonguk Kweon1,2, Jong-Min Suh1, Mi Hee Lim1, Dongwook Kim1,2 dwkxtal@kaist.ac.kr, Sukbok Chang1,2 sbchang@kaist.ac.kr
Publikováno v:
Science. 8/4/2023, Vol. 381 Issue 6657, p525-532. 8p. 6 Color Photographs.
Publikováno v:
ACS Catalysis. 13:4042-4052
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3bcb24dce8a106782254b2c33654bf45
https://doi.org/10.1021/acscatal.2c06303
https://doi.org/10.1021/acscatal.2c06303
Publikováno v:
ACS Catalysis. 12:8127-8138
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7959d23c16696a938396c7cfaeacd35
https://doi.org/10.1021/acscatal.2c02612
https://doi.org/10.1021/acscatal.2c02612
Publikováno v:
Journal of the American Chemical Society. 144:9161-9171
Herein, we report a photoinduced transition-metal-free C(aryl)-N bond formation between 2,4,6-tri(aryl)boroxines or arylboronic acids as an aryl source and 1,4,2-dioxazol-5-ones (dioxazolones) as an amide coupling partner. Chloride anion, either gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::940cf899def2d3d300b36d46a9f25281
https://doi.org/10.1021/jacs.2c03343
https://doi.org/10.1021/jacs.2c03343
Publikováno v:
Angewandte Chemie International Edition. 60:25235-25240
We report an approach for the intramolecular C(sp2 )-H amidation of N-acyloxyamides under photoredox conditions to produce δ-benzolactams with an aryl-alkyl σ-bond relocation. Computational studies on the designed reductive single electron transfer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ed71418cfc13d2cffd9d3e2f8e80d25
https://doi.org/10.1002/anie.202108775
https://doi.org/10.1002/anie.202108775
Autor:
Sukbok Chang, Gong Chen, Hao Wang, Shiyang Zhu, Gang He, Hoimin Jung, Fangfang Song, Danye Chen, Ziqian Bai
Publikováno v:
Nature Chemistry. 13:378-385
N-N linkages are found in many natural compounds and endow fascinating structural and functional properties. In comparison to the myriad methods for the construction of C-N bonds, chemistry for N-N coupling, especially in an intermolecular fashion, r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::570cf5b6d4ba77d3995c1f3eb6ae4ef0
https://doi.org/10.1038/s41557-021-00650-0
https://doi.org/10.1038/s41557-021-00650-0
Publikováno v:
Journal of the American Chemical Society. 142:8880-8889
The transition-metal-catalyzed nitrenoid transfer reaction is one of the most attractive methods for installing a new C-N bond into diverse reactive units. While numerous selective aminations are known, understanding complex structural effects of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e57492b0761f47f71702e3eeb1a5deb
https://doi.org/10.1021/jacs.0c02079
https://doi.org/10.1021/jacs.0c02079
Publikováno v:
Journal of the American Chemical Society. 142:5811-5818
Reported herein is the design of a photosensitization strategy to generate triplet nitrenes and its applicability for the intramolecular C–H amidation reactions. Substrate optimization by tuning ph...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::170b7ab343e2f06d9a826e9ac86f3c70
https://doi.org/10.1021/jacs.0c00868
https://doi.org/10.1021/jacs.0c00868
Publikováno v:
Chemical Science
Catalysis is central to contemporary synthetic chemistry. There has been a recent recognition that the rates of photochemical reactions can be profoundly impacted by the use of Lewis acid catalysts and co-catalysts. Herein, we show that Brønsted aci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02cc16bbca92381dd6383a9a2f386206
https://doi.org/10.1039/c9sc04822g
https://doi.org/10.1039/c9sc04822g
Publikováno v:
Angewandte Chemie International Edition. 58:7361-7365
Described herein is an unprecedented access to BN-polyaromatic compounds from 1,1'-biphenylamines by sequential borane-mediated C(sp2 )-H borylation and intramolecular N-demethylation. The conveniently in situ generated Piers' borane from a borinic a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d77c6f659bb4679fea96134c6a628574
https://doi.org/10.1002/anie.201902499
https://doi.org/10.1002/anie.201902499