Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Yan-Long Zheng"'
Publikováno v:
Chinese Medical Journal, Vol 129, Iss 20, Pp 2512-2513 (2016)
Externí odkaz:
https://doaj.org/article/4e31d13ee6e14a1a985c8c5127f6e63d
Publikováno v:
Chemical Communications. 59:2751-2754
A NiH-catalyzed polarity-reversed hydroamination of β,γ-, γ,δ- and δ,ε-unsaturated alkenes with anthranils was developed to access diverse arylamines bearing a carbonyl or alcohol functionality with 100% atom efficiency.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34c330c3917504b9bf4baec07c8de0c1
https://doi.org/10.1039/d2cc07052a
https://doi.org/10.1039/d2cc07052a
Publikováno v:
Chemical Science. 14:2040-2045
A direct, efficient and practical method for the three-component arylative coupling of aldehydes (or the corresponding alcohols), alkynes and arylboronic acids has been developed through nickel catalysis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c31e1faafd134a1151c8741df5f219d
https://doi.org/10.1039/d2sc05894d
https://doi.org/10.1039/d2sc05894d
Autor:
Yan-Long Zheng, Li Zhao, Yongqiang Li, Hongjian Song, Ding Yi, Yue Feng, Wenjie Tan, Qingmin Wang, Wenling Wang, Roujian Lu, Yuxiu Liu, Fei Ye, Xiangrong Song, Baoying Huang, Ziwen Wang, Wen Xiao
Publikováno v:
ACS Medicinal Chemistry Letters
The coronavirus disease 2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has stimulated the search for effective drugs for its prevention and treatment. Natural products are an important source for new d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee39e68e55a054c8e5817d201fdf563f
http://europepmc.org/articles/PMC8565188
http://europepmc.org/articles/PMC8565188
Autor:
Yan‐Long Zheng, Mengchun Ye
Publikováno v:
Chinese Journal of Chemistry. 38:489-493
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c099bf1a9ada53e97e79afe25d8fc35
https://doi.org/10.1002/cjoc.201900543
https://doi.org/10.1002/cjoc.201900543
Autor:
Stephen G. Newman, Yan-Long Zheng
Publikováno v:
Angewandte Chemie International Edition. 58:18159-18164
While esters are frequently used as traditional electrophiles in substitution chemistry, their application in cross-coupling chemistry is still in its infancy. This work demonstrates that methyl esters can be used as coupling electrophiles in Ni-cata
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6395277c66a0d1fbe725a3b7c7e948ea
https://doi.org/10.1002/anie.201911372
https://doi.org/10.1002/anie.201911372
Publikováno v:
Angewandte Chemie (International ed. in English). 60(24)
The direct conversion of alkyl esters to ketones has been hindered by the sluggish reactivity of the starting materials and the susceptibility of the product towards subsequent nucleophilic attack. We have now achieved a cross-coupling approach to th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::402be772799b183293a31bb67615945d
https://pubmed.ncbi.nlm.nih.gov/33792138
https://pubmed.ncbi.nlm.nih.gov/33792138
Autor:
Yan-Long Zheng, Stephen G. Newman
Publikováno v:
Chemical communications (Cambridge, England). 57(21)
Cross-coupling reactions to form biaryls and π bond addition reactions to prepare substituted carbonyls or alcohols represent two of the most frequently performed families of chemical reactions. Recent progress in catalysis has uncovered substantial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::022c9a7710da367556ac0ee4beca8268
https://pubmed.ncbi.nlm.nih.gov/33616584
https://pubmed.ncbi.nlm.nih.gov/33616584
Publikováno v:
Journal of the American Chemical Society. 142(18)
We report a one-step procedure to directly reduce unactivated aryl esters into their corresponding tolyl-derivatives. This is achieved by the action of a Ni/NHC catalyst and an organosilane reducing agent that is activated in situ by stoichiometric K
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::580680b2574f6f9cfd76c76b68c9e90f
https://pubmed.ncbi.nlm.nih.gov/32319766
https://pubmed.ncbi.nlm.nih.gov/32319766
Autor:
Mengchun Ye, You-Ge Pu, Jiang-Fei Li, Qi-Lin Zhou, Wei-Wei Yao, Xingwang Han, Tao Zhang, Yan-Long Zheng
Publikováno v:
Angewandte Chemie. 130:5162-5165
A Brønsted acid enabled nickel-catalyzed hydroalkenylation of aldehydes and styrene derivatives has been developed. The Brønsted acid acts as a proton shuttle to transfer a proton from the alkene to the aldehyde, thereby leading to an economical an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17c07109615a507558854ade630f1814
https://doi.org/10.1002/ange.201801817
https://doi.org/10.1002/ange.201801817