Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Ebrahim‐Alkhalil M. A. Ahmed"'
Autor:
Jiamin Fei, Shiqiang Zhao, Xiaoxu Bo, Furong Xie, Guanghui Li, Ebrahim‐Alkhalil M. A. Ahmed, Qingcheng Zhang, Huile Jin, Zhiqun Lin
Publikováno v:
Carbon Energy, Vol 5, Iss 8, Pp n/a-n/a (2023)
Abstract Hollow structuring has been identified as an effective strategy to enhance the cycling stability of electrodes for rechargeable batteries due to the outstanding volume expansion buffering efficiency, which motivates ardent pursuing on the sy
Externí odkaz:
https://doaj.org/article/8d32b63128124b118110b1c5a76a9641
Autor:
Furong Xie, Shiqiang Zhao, Xiaoxu Bo, Guanghui Li, Jiamin Fei, Ebrahim-Alkhalil M. A. Ahmed, Qingcheng Zhang, Huile Jin, Shun Wang, Zhiqun Lin
Publikováno v:
Journal of Materials Chemistry A. 11:53-67
A robust solvothermal-driven solid-to-solid transition strategy is developed to craft tartaric acid-capped ultrafine SnO2 encapsulated in graphene with outstanding lithium and sodium storage reversibility due to effectively inhibited Sn coarsening.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a9c5f0099fa02cba857a6b78eb4d2a07
https://doi.org/10.1039/d2ta07435d
https://doi.org/10.1039/d2ta07435d
Autor:
Huiling Zhu, Peng Liu, Hongxin Liu, Ebrahim-Alkhalil M. A. Ahmed, Xingen Hu, Juan Li, Hong-Ping Xiao, Xinhua Li, Jun Jiang
Publikováno v:
Organic Chemistry Frontiers. 9:2766-2772
Highly site- and enantio-selective additions of polyfunctional nucleophiles to imines or carbonyls were achieved via a carboxyl-assisted strategy, affording δ-substituted-β-keto esters and β-substituted ketones with good yield and enantioselectivi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0d513bfa3b28c56e8dada50262a3da9
https://doi.org/10.1039/d2qo00280a
https://doi.org/10.1039/d2qo00280a
Publikováno v:
Organic Letters. 23:3259-3263
Monofluoroalkenes normally act as metabolically stable bioisosteres for amide groups (-NH-CO-) and have widespread applications in drug discovery. Additionally, they are widely used as building blocks in organic synthesis. In this study, the Cu/Pd-ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e28d0543324e4af27e22d9d486d32b09
https://doi.org/10.1021/acs.orglett.1c00668
https://doi.org/10.1021/acs.orglett.1c00668
Publikováno v:
Chemical Communications. 57:6400-6403
Borylative difunctionalization of alkenes has emerged as a powerful approach for synthesizing highly functionalized molecules. Herein, dual Cu/Pd-catalysed borylfluoroallylation of alkenes was smoothly achieved by using gem-difluorinated cyclopropane
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::99bbfa66394e3e794452bce8caf323c9
https://doi.org/10.1039/d1cc01620b
https://doi.org/10.1039/d1cc01620b
Publikováno v:
Organic Letters. 22:1414-1419
Herein, we describe a palladium-catalyzed alkynylation of gem-difluorinated cyclopropanes via C–C bond activation/C–F bond cleavage, followed by C–C(sp) coupling. The new approach proceeds with broad substrate scope under mild reaction conditio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5bae75c8692d0b91bf26e71aa58a19cf
https://doi.org/10.1021/acs.orglett.0c00022
https://doi.org/10.1021/acs.orglett.0c00022
Publikováno v:
Organic Letters. 21:5645-5649
A palladium-catalyzed cross-coupling of gem-difluorinated cyclopropanes with boronic acids, providing the corresponding arylated/alkenylated/alkylated 2-fluoroallylic scaffolds, is generated. This new approach has good functional group compatibility
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37988126ec3612e1413375834b5ec6e9
https://doi.org/10.1021/acs.orglett.9b01979
https://doi.org/10.1021/acs.orglett.9b01979
Publikováno v:
Organic letters. 23(9)
Monofluoroalkenes normally act as metabolically stable bioisosteres for amide groups (-NH-CO-) and have widespread applications in drug discovery. Additionally, they are widely used as building blocks in organic synthesis. In this study, the Cu/Pd-ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d5f25c5df220cbbaf5e7922da86b541e
https://pubmed.ncbi.nlm.nih.gov/33872017
https://pubmed.ncbi.nlm.nih.gov/33872017
Autor:
Hong-Ping Xiao, Hongxin Liu, Jun Jiang, Ebrahim-Alkhalil M. A. Ahmed, Xingen Hu, Juan Li, Lingchen He
Publikováno v:
The Journal of organic chemistry. 86(6)
We described a Ni-bidentate oxazoline catalyzed highly enantio- and diastereoselective decarboxylative aldol reaction of 2-oxotetrahydrofuran-3-carboxylic acid/2-oxochromane-3-carboxylic acid derivatives with different kinds of carbonyls. Under optim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f27f9e65048c87211e8d62b0238df1b
https://pubmed.ncbi.nlm.nih.gov/33635652
https://pubmed.ncbi.nlm.nih.gov/33635652
Publikováno v:
Organic letters. 22(4)
Herein, we describe a palladium-catalyzed alkynylation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fd364daa9459a13ec42718c3c84f8b51
https://pubmed.ncbi.nlm.nih.gov/32011150
https://pubmed.ncbi.nlm.nih.gov/32011150