Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Runpu Shen"'
Autor:
Yanyu Ma, Xueyou Qin, Hui Yan, Junjie Li, Chengwei Li, Mingke Lian, Xuemei Wei, Runpu Shen, Mingyang Chen, Kangli Li, Junbo Gong
Publikováno v:
Crystals, Vol 13, Iss 8, p 1186 (2023)
The citrate industry has a wide range of applications in food, pharmaceutical, and other fields. As a common class of food additives and functional supplements with tremendous development potential and strong core competitiveness, particles with good
Externí odkaz:
https://doaj.org/article/2048b37b38e74cd6843b759a6bdcecaf
Publikováno v:
Molecules, Vol 22, Iss 8, p 1295 (2017)
A simple and efficient method for the synthesis of spiro[indoline-3,9′-xanthene]trione derivatives by means of condensation between isatins and 1,3-cyclohexanedione in the presence of a catalytic amount of magnesium perchlorate at 80 °C in 50% aqu
Externí odkaz:
https://doaj.org/article/8f903c18f2824220baf09281ebab86eb
Autor:
Xuemei, Wei, Kai, Wang, Guofeng, Wu, Guoqi, Yu, Hualiang, Shen, Tao, Cai, Yanjuan, Luo, Tianbo, Shang, Xinzhi, Chen, Runpu, Shen, Bin, Hu
Publikováno v:
Dalton Transactions: An International Journal of Inorganic Chemistry; 12/7/2024, Vol. 53 Issue 45, p18217-18225, 9p
Publikováno v:
The Journal of Organic Chemistry. 87:15114-15119
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66c44b56196e214f939ab85b7c66d011
https://doi.org/10.1021/acs.joc.2c01593
https://doi.org/10.1021/acs.joc.2c01593
Autor:
Zhebing Zhang, Tao Cai, Zhaohui Zhan, Huiting Xu, Lemao Yu, Xiang Luo, Chunmei Li, Yuzhen Gao, Xuemei Wei, Xinzhi Chen, Runpu Shen
Publikováno v:
Organic & Biomolecular Chemistry. 20:7221-7225
We developed a protocol for the preparation of valuable 5H-dibenzo[a,d]cycloheptenes by a formal [5 + 2] annulation of ortho-aryl alkynyl benzyl alcohols with arenes. Structurally diverse 5H-dibenzo[a,d]cycloheptenes were achieved in moderate to good
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1db995beb8695f6bc81f3a8a7bca49b1
https://doi.org/10.1039/d2ob01335e
https://doi.org/10.1039/d2ob01335e
Autor:
Mengqiang Luo, Yaohong Zhang, Ping Fang, Yan Li, Chenze Qi, Yong Li, Runpu Shen, Kai Cheng, Hai Wang
Publikováno v:
Organic & Biomolecular Chemistry. 20:630-635
An environmentally benign, cost-efficient and practical methodology for the room temperature synthesis of 2-arylacetophenones in water has been discovered.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5ba3132f121f105ceec95cbdb18b4db5
https://doi.org/10.1039/d1ob02023d
https://doi.org/10.1039/d1ob02023d
Autor:
Yaohong Zhang, Mengqiang Luo, Yichan Zhang, Kai Cheng, Yong Li, Chenze Qi, Runpu Shen, Hai Wang
Publikováno v:
Organic & Biomolecular Chemistry. 20:1952-1957
A facile and efficient oxidative functionalization of vinyl azides with aldehydes furnishing a diverse array of β-acylated enaminones was developed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18c5dbcb4866d75631555e7f3cd8d9c5
https://doi.org/10.1039/d1ob02479e
https://doi.org/10.1039/d1ob02479e
Publikováno v:
Advanced Synthesis & Catalysis. 364:766-772
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1a4a0261458f737585b4d9b3e7e6990
https://doi.org/10.1002/adsc.202101141
https://doi.org/10.1002/adsc.202101141
Autor:
Zhebing, Zhang, Tao, Cai, Zhaohui, Zhan, Huiting, Xu, Lemao, Yu, Xiang, Luo, Chunmei, Li, Yuzhen, Gao, Xuemei, Wei, Xinzhi, Chen, Runpu, Shen
Publikováno v:
Organicbiomolecular chemistry. 20(36)
A new synthetic methodology for the synthesis of 5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6a4fa27286a641cc196ffe924d78dfb2
https://pubmed.ncbi.nlm.nih.gov/36053155
https://pubmed.ncbi.nlm.nih.gov/36053155
Autor:
Kui Du, Minghao Sun, Jiehai Peng, Shaodong Zhou, Guodong Sheng, Runpu Shen, Liping Deng, Chunqi Hu, Yue Sun, Pengfei Zhang
Publikováno v:
Applied Surface Science. 625:157115
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09cb9724a8f28a0175efb8a441802382
https://doi.org/10.1016/j.apsusc.2023.157115
https://doi.org/10.1016/j.apsusc.2023.157115