Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Yin-Long Lai"'
Autor:
Liu-Liang Mao, An-Xi Zhou, Xian-Hong Zhu, Li-Xia Quan, Fayun Chen, Jie-Ping Wan, Yin-Long Lai
Publikováno v:
Organic & Biomolecular Chemistry. 20:1196-1199
An efficient visible-light-mediated tandem phosphorylation/cyclization of N-arylacrylamides with H-phosphine oxides is described, providing a series of phosphorylated oxindoles in good yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28aeff068bac772770594a6c0ea16564
https://doi.org/10.1039/d1ob02486h
https://doi.org/10.1039/d1ob02486h
Publikováno v:
European Journal of Organic Chemistry. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9fd5fc6d57babfc3d198e68181c7457
https://doi.org/10.1002/ejoc.202201387
https://doi.org/10.1002/ejoc.202201387
Autor:
Yin‐Long Lai, Xiao Yang, Si‐Chao Wu, Xi‐Yong Li, Yao‐Xiong Gong, Sheng‐Ling Zhang, Rui‐Min Zhong, Jian‐Hua Liao, Jian‐Min Luo (Dr.)
Publikováno v:
ChemElectroChem. 9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::566710bdf3502b43d0123401bd3a3b69
https://doi.org/10.1002/celc.202200787
https://doi.org/10.1002/celc.202200787
Autor:
Yin‐Long Lai, Shao‐Xi Yan, Sheng‐Ling Zhang, Yu‐Hong Huang, Ru‐Xin Hu, Yang‐Chong Chen, Jian‐Min Luo, Jianxiao Li
Publikováno v:
Chemistry – An Asian Journal. 17
A reliable and efficient palladium-catalyzed cascade cyclization/alkylation of oxime ethers with unactivated alkenes is described, affording a whole variety of structurally diverse isoxazole derivatives in moderate to good yields with excellent funct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58afe799d3f85349f706bc1ca79cc2d7
https://doi.org/10.1002/asia.202200806
https://doi.org/10.1002/asia.202200806
Publikováno v:
Asian Journal of Organic Chemistry. 10:711-748
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7de463b9e7affb7c0a43873e127deadb
https://doi.org/10.1002/ajoc.202100009
https://doi.org/10.1002/ajoc.202100009
Publikováno v:
RSC advances. 11(46)
An efficient and straightforward palladium-catalyzed three-component cascade bisthiolation of terminal alkynes and arylhydrazines with sodium thiosulfate (Na
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::460f5a4ae3567d4107cecc7662bf1223
https://pubmed.ncbi.nlm.nih.gov/35478536
https://pubmed.ncbi.nlm.nih.gov/35478536
Publikováno v:
ChemElectroChem. 6:4188-4193
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0cb81b0c82109420b763a17520b1c577
https://doi.org/10.1002/celc.201801502
https://doi.org/10.1002/celc.201801502
Autor:
Yin-Long, Lai, Yunyan, Mo, Shaoxi, Yan, Shengling, Zhang, Lejie, Zhu, Jianmin, Luo, Huishi, Guo, Jianpeng, Cai, Jianhua, Liao
Publikováno v:
RSC advances. 10(55)
An efficient electrochemical transformation of a variety of alkenes and sulfonyl hydrazides into vinyl sulfones with a catalytic amount of tetrabutylammonium iodide in water is reported. The reaction proceeds smoothly to afford vinyl sulfones with go
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9dca135994f5ac12274a4448d8620181
https://pubmed.ncbi.nlm.nih.gov/35515034
https://pubmed.ncbi.nlm.nih.gov/35515034
Publikováno v:
Chemistry - A European Journal. 22:5425-5429
An electrochemical synthesis of benzazoles directly from alcohols and o-substituted anilines has been developed. The reaction conditions have been optimized by varying the composition of the electrolyte and the metal salt used as catalyst. The cycliz
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eece4c651e3e84986c0128d96393a107
https://doi.org/10.1002/chem.201505074
https://doi.org/10.1002/chem.201505074
Publikováno v:
The Journal of organic chemistry. 82(18)
A stereoselective synthesis of (E)-vinyl sulfones has been developed via electrochemical oxidative N–S bond cleavage of aromatic sulfonylhydrazides, followed by cross-coupling reactions with cinnamic acids to form the C–S bond. The protocol proce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34aa2e61f0b196511e454a7e74b8fc74
https://pubmed.ncbi.nlm.nih.gov/28853571
https://pubmed.ncbi.nlm.nih.gov/28853571