Zobrazeno 1 - 10
of 78
pro vyhledávání: '"Pu-Sheng Wang"'
Autor:
Yu Yang, Cheng Zhang, Chengyi Zhang, Yaohui Shi, Jun Li, Bernt Johannessen, Yongxiang Liang, Shuzhen Zhang, Qiang Song, Haowei Zhang, Jialei Huang, Jingwen Ke, Lei Zhang, Qingqing Song, Jianrong Zeng, Ying Zhang, Zhigang Geng, Pu-Sheng Wang, Ziyun Wang, Jie Zeng, Fengwang Li
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-11 (2024)
Abstract Cu catalyses electrochemical CO2 reduction to valuable multicarbon products but understanding the structure-function relationship has remained elusive due to the active Cu sites being heterogenized and under dynamic re-construction during el
Externí odkaz:
https://doaj.org/article/a12eac01c620445cb8963c36d093c9ec
Publikováno v:
Tetrahedron Chem, Vol 1, Iss , Pp 100002- (2022)
An enantio- and diastereodivergent [2+2+1] annulation reaction of allyl ketones, acidic methylene compounds, and nitroalkenes to assemble highly functionalized cyclopentanes from readily available substances enabled by asymmetric relay catalysis of c
Externí odkaz:
https://doaj.org/article/aeff038808e2419eba1345b08d62f6ec
Publikováno v:
Organic Letters. 25:210-214
The diverse functionalization of 1,3-butadiene provides wide applicability toward the synthesis of abundant and useful allylic compounds. Here, we describe a three-component and redox-neutral assembly of readily available C═X compounds, 1,3-butadie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97a43931f885fa7a95403da50a7acdbb
https://doi.org/10.1021/acs.orglett.2c04060
https://doi.org/10.1021/acs.orglett.2c04060
Publikováno v:
Nature Synthesis. 1:946-955
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::47d70263e8cf4a9fe78d7977fb526880
https://doi.org/10.1038/s44160-022-00172-8
https://doi.org/10.1038/s44160-022-00172-8
Autor:
Pu‐Sheng Wang, Liu‐Zhu Gong
Publikováno v:
Chinese Journal of Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19a895b92d66320bd6749890229d8e8e
https://doi.org/10.1002/cjoc.202300063
https://doi.org/10.1002/cjoc.202300063
Autor:
Pu-Sheng Wang, Liuzhu' Gong
Pd-catalyzed asymmetric allylic C−H functionalization has emerged as a powerful tool to access chiral, densely functionalized molecules from easily ac-cessible alkenes, enabling the increase of the step- or atom-economy by minimizing functional gro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::160c1f892d26bdc7ba9dcaf22eebe620
https://doi.org/10.22541/au.167783107.70839118/v1
https://doi.org/10.22541/au.167783107.70839118/v1
Publikováno v:
Nature Synthesis. 1:487-496
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e778b1d40c1763526ddc321548d357b
https://doi.org/10.1038/s44160-022-00084-7
https://doi.org/10.1038/s44160-022-00084-7
Publikováno v:
Chem Catalysis. 2:1211-1222
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb0a21a35b04c7e3e5fcb520cb695f77
https://doi.org/10.1016/j.checat.2022.03.020
https://doi.org/10.1016/j.checat.2022.03.020
Publikováno v:
Journal of the American Chemical Society. 143:20454-20461
Asymmetric functionalization of the C(sp3)-H bond is an attractive yet challenging strategy to achieve versatile bond-forming events, enabling the precise assembly of molecular complexity with minimal manipulation of functional groups. Here, we repor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ece68d9ed85584a2e55e697631ec2516
https://doi.org/10.1021/jacs.1c10721
https://doi.org/10.1021/jacs.1c10721
Publikováno v:
Science China Chemistry. 65:298-303
Chiral homoallylic vicinal diols are found in many bioactive compounds and are among the most versatile functional groups in organic chemistry. Here, we describe an asymmetric carbonyl allylation of aldehydes with allyl ethers proceeding via allylic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e21d0ad36526d0247c263da8332fe8ec
https://doi.org/10.1007/s11426-021-1134-x
https://doi.org/10.1007/s11426-021-1134-x