Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Erqing Li"'
Autor:
Yijun Mao, Yuqiong Shi, Wenfang Qiao, Zhuo Zhang, Wei Yang, Haili Liu, Erqing Li, Hui Fan, Qiang Liu
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 11 (2024)
BackgroudAcute myocardial infarction (AMI) has a high morbidity rate, high mortality rate, high readmission rate, high health care costs, and a high symptomatic, psychological, and economic burden on patients. Patients with AMI usually present with m
Externí odkaz:
https://doaj.org/article/111cb7f1b322486cb611310bd94022f6
Publikováno v:
Journal of Materials Chemistry C. 10:6036-6042
The as-prepared SiO2@diarylethene/lanthanide complex hybrid material exhibits reversible luminescence switching behavior under alternating UV and visible light irradiation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a76eed8def728c796f0021ff15d2a523
https://doi.org/10.1039/d2tc00073c
https://doi.org/10.1039/d2tc00073c
Publikováno v:
Organic Chemistry Frontiers. 9:19-24
Herein we report a diastereodivergent synthesis of fully disubstituted spiro[indoline-3,2′-pyrrolidin]-2-ones through base-promoted (3 + 2) cycloadditions. Importantly, the catalysts are found to have full control over the configuration of the ster
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c12e8664b8ec3a06128fa57146525511
https://doi.org/10.1039/d1qo01124c
https://doi.org/10.1039/d1qo01124c
Publikováno v:
Organic Letters. 23:3094-3099
Herein we reported a novel phosphine-catalyzed (4 + 2) cyclization reaction of electron-deficient conjugated dienes with enones to generate functionalized dihydropyran skeletons. A mechanistic investigation reveals that the reaction produces a new ph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4056193bca1f22da90693f8a10ecded
https://doi.org/10.1021/acs.orglett.1c00780
https://doi.org/10.1021/acs.orglett.1c00780
Publikováno v:
Synthesis. 53:1331-1340
A highly efficient copper/GanPhos-catalyzed 1,3-dipolar cycloaddition of azomethine ylides is reported. This viable transformation provides a series of optically active spiro[dihydronaphthalene-2,3′-pyrrolidine]s, bearing one spiro quaternary a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7578f1d2e884c296e825a032778a8fc7
https://doi.org/10.1055/s-0040-1706599
https://doi.org/10.1055/s-0040-1706599
Publikováno v:
Advanced Synthesis & Catalysis. 362:4010-4026
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc3f34373ce8172bc63858178135e166
https://doi.org/10.1002/adsc.202000608
https://doi.org/10.1002/adsc.202000608
Publikováno v:
Asian Journal of Organic Chemistry. 9:1179-1182
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8afdaedae1d9525ad4ccfbf078c7ae95
https://doi.org/10.1002/ajoc.202000246
https://doi.org/10.1002/ajoc.202000246
Publikováno v:
The Journal of Organic Chemistry. 85:14772-14778
A simple method to build phospholene derivatives has been achieved in a one-pot reaction with readily available o-alkynylaryl bromides and alkylphosphine oxides. This method is also applicable to s...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d231d212d1321b0bb5fc456b2ee5f5f2
https://doi.org/10.1021/acs.joc.0c00545
https://doi.org/10.1021/acs.joc.0c00545
Publikováno v:
Organic & Biomolecular Chemistry. 18:646-649
A silver/palladium relay catalyzed 1,3-dipole annulation/allylation reaction of iminoesters and Baylis-Hillman acetates for the construction of fully substituted allyl imidazolidines is reported. The reaction of both iminoesters and Baylis-Hillman ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7bdd96791770f80746e238251f89c6c
https://doi.org/10.1039/c9ob02633a
https://doi.org/10.1039/c9ob02633a
Autor:
Zheng Duan, Manman Song, Donghui Wei, Yue Wang, Ke Li, Hao Cui, Congcong Wang, François Mathey, Erqing Li
Publikováno v:
Organic & Biomolecular Chemistry. 18:3740-3746
A copper-catalyzed asymmetric 1,3-dipolar cycloaddition of glycine iminoesters with alkyl substituted 3-methylene-2-oxindoles is described. By using de novo design of P-stereogenic phosphines as ligands, spiro[pyrrolidin-3,3'-oxindole]s are generated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d029e93b859e514dea667cec7f904cbc
https://doi.org/10.1039/d0ob00546k
https://doi.org/10.1039/d0ob00546k