Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Tiezheng Jia"'
Autor:
Kaiming Han, Hong Liu, Madeline E. Rotella, Zeyu Xu, Lizhi Tao, Shufeng Chen, Marisa C. Kozlowski, Tiezheng Jia
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-9 (2024)
Abstract The unique features of the sulfenamides’ S(II)-N bond lead to interesting stereochemical properties and significant industrial functions. Here we present a chemoselective Chan–Lam coupling of sulfenamides to prepare N-arylated sulfenamid
Externí odkaz:
https://doaj.org/article/952c3a14d5c049e2951b1c177f6201a1
Autor:
Cong Wang, Hui Zhang, Lucille A. Wells, Tian Liu, Tingting Meng, Qingchao Liu, Patrick J. Walsh, Marisa C. Kozlowski, Tiezheng Jia
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-11 (2021)
N-Arylation of NH-diaryl sulfoximines faces synthetic challenges among reported methods. Here, the authors present a mild copper-catalyzed photoredox dehydrogenative Chan-Lam coupling of free diaryl sulfoximines and arylboronic acids via an auto-cata
Externí odkaz:
https://doaj.org/article/b3b7c585ed974409961529e6bcd67547
Autor:
Guolin Li, Yexenia Nieves-Quinones, Hui Zhang, Qingjin Liang, Shuaisong Su, Qingchao Liu, Marisa C. Kozlowski, Tiezheng Jia
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-9 (2020)
Cross-coupling processes without the use of transition metals are challenging to achieve. Here, the authors show a transition-metal-free cross-coupling utilizing aryl(heteroaryl) methyl sulfoxides and alcohols to afford alkyl aryl(heteroaryl) ethers
Externí odkaz:
https://doaj.org/article/1679d5adbdd047cb86a6aaee0fff8c7d
Publikováno v:
ACS Medicinal Chemistry Letters. 13:1739-1744
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b738a5f8ee254a31951f80fff9e7ef4
https://doi.org/10.1021/acsmedchemlett.2c00348
https://doi.org/10.1021/acsmedchemlett.2c00348
Publikováno v:
Synlett. 34:429-432
As a promising pharmacophore, sulfondiimines have drawn increasing attention in recent years, but their uptake in medicinal chemistry is jeopardized by the scarcity of related transformations. Herein, we report a facile and mild N-alkylation protocol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f886ad91ad063c065ea7662b65fa615f
https://doi.org/10.1055/a-1946-6522
https://doi.org/10.1055/a-1946-6522
Autor:
Tingting Meng, Lucille A. Wells, Tianxin Wang, Jinyu Wang, Shishuo Zhang, Jie Wang, Marisa C. Kozlowski, Tiezheng Jia
Publikováno v:
Journal of the American Chemical Society. 144:12476-12487
Inspired by the discovery of a S═N bond in the collagen IV network and its essential role in stabilizing basement membranes, sulfilimines have drawn much attention in the fields of chemistry and biology. However, their further uptake is hindered by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f7fe129a7b6817aa5fb206868301e61
https://doi.org/10.1021/jacs.2c04627
https://doi.org/10.1021/jacs.2c04627
Autor:
Qingjin Liang, Tiezheng Jia
Publikováno v:
Advanced Synthesis & Catalysis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::044d59195efa2f9ef646c7bf1a5b13d2
https://doi.org/10.1002/adsc.202300320
https://doi.org/10.1002/adsc.202300320
Autor:
qingjin liang, Xinping Zhang, Madeline E. Rotella, Zeyu Xu, Marisa C. Kozlowski, Tiezheng Jia
Chan-Lam coupling constructs C-N, C-O and C-S bonds by coupling nucleophiles with boronic acids using copper complexes. Such methods benefit from inexpensive and sustainable catalysts, simple and mild reaction conditions, and the potential to generat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f22a89d6cee870c13a84332d737ab222
https://doi.org/10.21203/rs.3.rs-2779487/v1
https://doi.org/10.21203/rs.3.rs-2779487/v1
Publikováno v:
Trends in Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e5ce2b0ac834b5ae2ee435dc38077372
https://doi.org/10.1016/j.trechm.2023.03.003
https://doi.org/10.1016/j.trechm.2023.03.003
Publikováno v:
Advanced Synthesis & Catalysis. 364:2040-2046
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::183b4869db18925d7d7c1bd82577c881
https://doi.org/10.1002/adsc.202200279
https://doi.org/10.1002/adsc.202200279