Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jinghong Pu"'
Publikováno v:
ChemistrySelect. 3:12219-12222
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9b56e20d2e165988b215d3068d61856
https://doi.org/10.1002/slct.201802735
https://doi.org/10.1002/slct.201802735
Publikováno v:
Organic Chemistry Frontiers. 5:361-365
A novel and efficient CBr4-mediated oxidative cross-coupling reaction of α-amino carbonyl compounds with alcohols and thiols to build C–O and C–S bonds, respectively, has been developed. The reactions were realized under mild and transition-meta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7bef75e9589885417d44441beeee2d79
https://doi.org/10.1039/c7qo00830a
https://doi.org/10.1039/c7qo00830a
Autor:
Pengbo Jiang, Xinfeng Cui, Haojie Ma, Zhenzhen Zhan, Guosheng Huang, Yixin Zhang, Jinghong Pu
Publikováno v:
Organicbiomolecular chemistry. 17(20)
We have designed a general, inexpensive, and versatile method for the synthesis of (1H-benzo[d]imidazol-2-yl)(phenyl)methanone and the formation of C-N bonds via an aromatic aldehyde and o-phenylenediamine. In the presence of N,N-dimethylformamide/su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::782def36703dc3f1c8dda096e116a609
https://pubmed.ncbi.nlm.nih.gov/31073576
https://pubmed.ncbi.nlm.nih.gov/31073576
Autor:
Guosheng Huang, Daidong Wei, Wan‐Fa Tian, Xinliang Luo, Xingxing Liu, Xiaoqiang Zhou, Jinghong Pu
Publikováno v:
ChemistrySelect. 2:8658-8660
A new strategy for the synthesis of 3-phenylquinoline through annulation of azides with aldehydes has been established. The transformation was accomplished by palladium-catalyzed C−H functionalization and C−C bond cleavage to form two C−C bonds
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29570bf473b8cab2666e1e2d97321ae8
https://doi.org/10.1002/slct.201701312
https://doi.org/10.1002/slct.201701312
Autor:
Guosheng Huang, Xingxing Liu, Xinfeng Cui, Yixin Zhang, Shao-Hua Wang, Zhenzhen Zhan, Haojie Ma, Jinghong Pu
Publikováno v:
Organicbiomolecular chemistry. 16(24)
A novel [3 + 2] cycloaddition reaction of azaoxyallyl cations and aromatic ethylenes has been developed to afford multi-substituted pyrrolidinones in moderate to good yields. This method not only further expands the synthetic utility of α-halo hydro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7373ab12e893a0a6c38edcf1e85633a
https://pubmed.ncbi.nlm.nih.gov/29855642
https://pubmed.ncbi.nlm.nih.gov/29855642