Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Wenkui Lu"'
Autor:
Tingjuan He, Meixia Wang, Hongfei Mi, Liansheng Xu, Wenkui Lu, Xue Ouyang, Zhinan Guo, Chenghao Su
Publikováno v:
Vaccines, Vol 11, Iss 3, p 532 (2023)
Objective: Vaccine effectiveness can measure herd immunity, but the effectiveness of inactivated vaccines in Xiamen remains unclear. Our study was designed to understand the herd immunity of the COVID-19 inactivated vaccine against the SARA-CoV-2 Del
Externí odkaz:
https://doaj.org/article/8a6817e6931d443f9491629f0fac9567
Publikováno v:
ACS Catalysis. 11:10190-10197
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5054e8a582ae042d4082330b12b3b59a
https://doi.org/10.1021/acscatal.1c02129
https://doi.org/10.1021/acscatal.1c02129
Publikováno v:
Organometallics. 39:3780-3788
Direct synthesis of arylalkenylsilanes by [Rh(COD)Cl]2/PPh3-catalyzed dehydrogenative silylation of styrene derivatives with R3SiH (R = alkyl, alkoxy, aryl) was realized, in which norbornene (NBE) ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec30c0a9ec73f3d3a796de65a3a0b085
https://doi.org/10.1021/acs.organomet.0c00242
https://doi.org/10.1021/acs.organomet.0c00242
Publikováno v:
Open medicine (Warsaw, Poland). 17(1)
In this study, we aim to investigate moscatilin in alleviating symptoms of autoimmune liver disease (ALD) in a concanavalin A (ConA)-induced liver injury mouse model and elucidate the underlying mechanisms. ALD mouse models were constructed by intrav
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00315af7fa2bb62ea86c002605427138
https://pubmed.ncbi.nlm.nih.gov/35509689
https://pubmed.ncbi.nlm.nih.gov/35509689
Publikováno v:
The Journal of Organic Chemistry. 84:16086-16094
The asymmetric hydrogenation of 2,4-pentadien-1-ones has been achieved by using trans-RuCl2[(R)-XylylSunPhos][(R)-Daipen] as a catalyst under basic conditions. This hydrogenation demonstrated exclusive C1-carbonyl selectivity, and thus the conjugated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9aaa7cdf9ecbf4e14ba7e6344aaafd21
https://doi.org/10.1021/acs.joc.9b02576
https://doi.org/10.1021/acs.joc.9b02576
Autor:
Xiaomin Xie, Jingyang Wang, Guangni Ding, Zhaoguo Zhang, Wenkui Lu, Liqun Yang, Xiaoyu Wu, Yuxuan Zhang
Publikováno v:
Organic letters. 23(4)
We report a simple and effective nickel-based catalytic system, NiCl2·6H2O/tBuOK, for the electrophilically activated hydrosilylation of terminal alkenes with primary silanes. This protocol provides excellent performance under mild reaction conditio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::960ee6d79ef5cee7eaae467ef38bde2d
https://pubmed.ncbi.nlm.nih.gov/33522233
https://pubmed.ncbi.nlm.nih.gov/33522233
Publikováno v:
Tetrahedron. 109:132632
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6fd90d4dcc0fed6c8e44eb29d29ffa7c
https://doi.org/10.1016/j.tet.2022.132632
https://doi.org/10.1016/j.tet.2022.132632
Autor:
Zengming Shen, Wenkui Lu
Publikováno v:
Organic Letters. 21:142-146
We report an efficient approach for the direct synthesis of alkenylboronates using copper catalysis. The Cu/TEMPO catalyst system (where TEMPO = (2,2,6,6-tetramethylpiperidin-1-yl)oxyl) exhibits both excellent reactivity and selectivity for the synth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e03a2a818f4c0c02600b2b32b6e52c8
https://doi.org/10.1021/acs.orglett.8b03599
https://doi.org/10.1021/acs.orglett.8b03599
Publikováno v:
Organic Letters. 20:5610-5613
An alkoxide-catalyzed hydrosilylation of cyclic imides to isoquinolines was realized via tandem reduction and rearrangement. Using TMSOK as the catalyst and (EtO)2MeSiH as the reductant, a series of cyclic imides containing different functional group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::928e98f2346a8a682e1175c1375fe6d0
https://doi.org/10.1021/acs.orglett.8b02287
https://doi.org/10.1021/acs.orglett.8b02287
Publikováno v:
Tetrahedron. 74:1144-1150
B(C6F5)3-catalyzed hydrosilylation of cyclic imides afforded an efficient synthetic method of pyrrolidines. In the presence of 5 mol% B(C6F5)3, various aromatic, aliphatic and polycyclic imides were smoothly reduced by PhSiH3 to generate the correspo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::681211c0f3ac2177bcf48344d805d909
https://doi.org/10.1016/j.tet.2018.01.051
https://doi.org/10.1016/j.tet.2018.01.051