Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Xiufang Cheng"'
Autor:
Yong Zhang, Qi Jiang, Yuan Yuan, Yi Zhao, Na Chen, Yawen Li, Hui Peng, Junping Liu, Yanli Li, Jing Wei, Fu Xiong, Huimin Zhang, Yanhong Liu, Guochang Xue, Huali Zhang, Xuexing Ding, Changlin Wang, Huili Yan, Mingxing Ren, Chaoying Ma, Hanming Lu, Ruifeng Meng, Lingjun Xie, Xiufang Cheng, Jiaojiao Wang, Xiaohong Xin, Ruifen Wang, Guijuan Liang, Yuanzheng Li, Jianing Kang, Yinying Zhang, Yinglin Su, Shengjie Duan, Qingsheng Liu
Publikováno v:
BMJ Paediatrics Open, Vol 7, Iss 1 (2023)
Background Since most infants are usually discharged before age 48–72 hours, peak bilirubin levels will almost always occur after discharge. Parents may be the first to observe the onset of jaundice after discharge, but visual assessment is unrelia
Externí odkaz:
https://doaj.org/article/eb52cd3dfd8c40a9ac5f4e7e34076ae3
Autor:
Xiufang Cheng, Chao Zhang
Publikováno v:
Jixie chuandong, Vol 43, Pp 95-98 (2019)
With the increasing of temporomandibular joint disorder syndrome and the increasing number of patients with oral external trauma，the development of the mandibular rehabilitation robot is very important. In order to meet the training requirements of
Externí odkaz:
https://doaj.org/article/23cf9f00bf8443d099db69795ae6bf1d
Publikováno v:
RSC Advances. 12:35649-35654
γ-Keto sulfones are versatile building blocks and valuable intermediates in organic synthesis and pharmaceutical chemistry. Motivated by their excellent properties, we herein report a green, convenient, metal-free hydrosulfonylation method for a var
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7fe0124dc01e4c835ed0430c6000bca
https://doi.org/10.1039/d2ra06784f
https://doi.org/10.1039/d2ra06784f
Publikováno v:
Green Chemistry. 18:5773-5776
An efficient procedure for the synthesis of 2-arylquinazolines from N′-arylbenzimidamides has been developed under transition-metal-free conditions. In this process, stable and low-toxicity paraformaldehyde was used as the carbon source. A broad ra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2eebcdfb5edc594379a299bdb03ae6f3
https://doi.org/10.1039/c6gc02319c
https://doi.org/10.1039/c6gc02319c
Publikováno v:
Journal of Information Processing Systems; Jun2021, Vol. 17 Issue 3, p462-472, 11p
Publikováno v:
Green Chemistry. 17:209-213
An efficient procedure for 4,5-dihydro-1H-imidazol-5-one preparation from aryl amidines and ketones under transition-metal free conditions is described. When cyclic ketones were employed, various spiro-fused 4,5-dihydro-1H-imidazol-5-ones were formed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e93d679c7cb8504057ea60ef68e35f2
https://doi.org/10.1039/c4gc01515k
https://doi.org/10.1039/c4gc01515k
Publikováno v:
Green Chem.. 16:4644-4648
A transition-metal-free method for the synthesis of 2-arylbenzoxazoles from readily available cyclohexanones and benzamides is described. The combined use of KI, p-TsOH and DMSO significantly improved the reaction yields. Non-aromatic cyclohexanones
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::17f907bf875839ecd7d24eeec64f8754
https://doi.org/10.1039/c4gc01572j
https://doi.org/10.1039/c4gc01572j
Publikováno v:
ChemInform. 47
2-Aroylbenzofurans are efficiently prepared based on an in situ formylation reaction using cheap and stable paraformaldehyde as carbon source.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::195b6efc146483bf2736187e8cacc21c
https://doi.org/10.1002/chin.201628128
https://doi.org/10.1002/chin.201628128
Publikováno v:
Organicbiomolecular chemistry. 14(10)
An efficient procedure for 2-aroylbenzofuran preparation from 2-bromophenols, phenacyl bromides and paraformaldehyde is described. The cheap and stable paraformaldehyde served as the carbon source via an in situ formylation reaction.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ffed23dc7f86328629c0a8820212848
https://pubmed.ncbi.nlm.nih.gov/26864606
https://pubmed.ncbi.nlm.nih.gov/26864606