Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Kuiyong, Dong"'
Autor:
Kuiyong Dong, Xing Fan, Chao Pei, Yang Zheng, Sailan Chang, Ju Cai, Lihua Qiu, Zhi-Xiang Yu, Xinfang Xu
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-10 (2020)
The formation of chiral molecules generally relies on direct chirality transfer from catalyst to products. Here, the authors report a strategy based on point chirality transfer from the catalyst to a dirhodium carbene intermediate with axial chiralit
Externí odkaz:
https://doaj.org/article/6609708ced464bc581ae42daa272f2d5
Autor:
Kostiantyn O. Marichev, Kuiyong Dong, Lynée A. Massey, Yongming Deng, Luca De Angelis, Kan Wang, Hadi Arman, Michael P. Doyle
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-10 (2019)
Chiral 3-azetidinones are structural analogues of medicinally relevant β-lactams, however their synthesis and reactivity are underexplored. Here, the authors show a highly enantioselective copper-catalyzed [3 + 1]-cycloaddition generating 2-azetidin
Externí odkaz:
https://doaj.org/article/2224efd87e00455cbf9a7b670366ac96
Publikováno v:
Molecules, Vol 27, Iss 10, p 3088 (2022)
As one of the abundant and inexpensive metals on the earth, copper has demonstrated broad applications in synthetic chemistry and catalysis. Among these copper-catalyzed advances, copper carbenes are versatile and reactive intermediates that can medi
Externí odkaz:
https://doaj.org/article/2b094916d53a43d3b6f1ee8658f475a5
Publikováno v:
Organicbiomolecular chemistry. 20(42)
A copper-catalyzed three-component reaction of dithioacetals with diazo-ketones and ketimines has been reported. This reaction proceedsivia/itrapping of the highly active sulfur ylide species, which are generated from thioacetal and carbene intermedi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63f81bbc12a4fb66673c1cceff7ecb72
https://pubmed.ncbi.nlm.nih.gov/36250291
https://pubmed.ncbi.nlm.nih.gov/36250291
Generation of Diazomethyl Radicals by Hydrogen Atom Abstraction and Their Cycloaddition with Alkenes
Publikováno v:
Angewandte Chemie International Edition. 60:18484-18488
A general catalytic methodology for the synthesis of pyrazolines from α -diazo compounds and conjugated alkenes is reported. The direct hydrogen atom transfer (HAT) process of α -diazo compounds promoted by the tert -butylperoxy radical generates e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34183dd9de63e8f3379a2917d2e9c94f
https://doi.org/10.1002/anie.202105472
https://doi.org/10.1002/anie.202105472
Autor:
Michael P. Doyle, Wendell P. Griffith, Ahmad Humeidi, Xinfang Xu, Kuiyong Dong, Hadi D. Arman
Publikováno v:
Angewandte Chemie. 133:13506-13512
An unprecedented Ag(I)-catalyzed efficient method for the coupling of β-oxoimides and enol diazoacetates through a [3+2]-cycloaddition/C-O bond cleavage/[1,5]-proton transfer cascade process is reported. The general class of imino ethers that includ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f19088c9eca9ad69653f2b3a66cbe52
https://doi.org/10.1002/ange.202101641
https://doi.org/10.1002/ange.202101641
Autor:
Haifeng Zheng, Ahmad Humeidi, Hadi D. Arman, Kuiyong Dong, Xinfang Xu, Yong-Liang Su, Michael P. Doyle
Publikováno v:
ACS Catalysis. 11:4712-4721
Catalyst-directed access to divergent products involving three different metals that exclusively form three different products from the same reactants is reported. Each catalyst directs an individu...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd03a0e1736722a958d3c04a2439f9a9
https://doi.org/10.1021/acscatal.1c01051
https://doi.org/10.1021/acscatal.1c01051
Autor:
Kan Wang, Jinzhou Chen, Michael P. Doyle, Jinping Lei, Kuiyong Dong, Kostiantyn O. Marichev, Nicole Greco
Publikováno v:
Chemistry – A European Journal. 27:340-347
1,2,3-Trisubstituted donor-acceptor cyclopropenes (DACPs) generated in situ from enoldiazo compounds react with nucleophiles to form α-substituted succinic acid derivatives in high yields. Initial dirhodium(II) carboxylate catalysis rapidly converts
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62c204f8104e2e00d8fa740a7a62a5d6
https://doi.org/10.1002/chem.202003427
https://doi.org/10.1002/chem.202003427
Publikováno v:
Advanced Synthesis & Catalysis. 362:3137-3141
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72826eeba959ac45b67939f47c6943dc
https://doi.org/10.1002/adsc.202000360
https://doi.org/10.1002/adsc.202000360
Publikováno v:
Organic Chemistry Frontiers. 7:1653-1657
Chiral copper(I) catalysts are preferred over chiral dirhodium(II) catalysts for [3 + 3]-cycloaddition reactions of γ-alkyl-substituted enoldiazoacetates compounds with nitrones. Using the In-SaBox ligand these reactions effectively produce cis-3,6-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a933b9d6fc9412d976d2bd4dedc5a41
https://doi.org/10.1039/d0qo00539h
https://doi.org/10.1039/d0qo00539h