Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Guoling Huang"'
Autor:
Dongmei Xu, Jie You, Guixia Chen, Hongli Su, Li Zhang, Lingling Cui, Zhonglei Li, Guoling Huang, Caiying Feng
Publikováno v:
Journal of Diabetes Research, Vol 2021 (2021)
Previous studies have discovered that zinc-α2-glycoprotein (ZAG) is related to insulin resistance and lipid metabolism. The aim of the study is to explore the change of serum ZAG and its related factors in gestational diabetes mellitus (GDM). Eighty
Externí odkaz:
https://doaj.org/article/bd56f706cc3547798884a9e388c37e5c
Publikováno v:
Organic Letters. 25:3179-3183
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af656009fd5b6c8fc50934db1a6532da
https://doi.org/10.1021/acs.orglett.3c01077
https://doi.org/10.1021/acs.orglett.3c01077
Publikováno v:
Organic & Biomolecular Chemistry. 21:3547-3551
Herein, we report an efficient non-radical protocol to construct NH-free C-3 bifunctional oxindoles through a Rh(ii) catalyzed intermolecular [2,3]-sigmatropic rearrangement reaction between diazooxindoles and tertiary allylic amines.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a62065f9817b465b7eff9c8c6322b726
https://doi.org/10.1039/d3ob00478c
https://doi.org/10.1039/d3ob00478c
Inhere, the first instance of copper-catalyzed oxidative amination of sulfenamides for the synthesis of sulfinamidines was documented. Employing air as the terminal oxidant, a variety of secondary and primary amines can be effectively transformed int
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b12a9f31b920bd11b344231a167200d
https://doi.org/10.26434/chemrxiv-2023-31393-v2
https://doi.org/10.26434/chemrxiv-2023-31393-v2
This study presents a novel, efficient method for the synthesis of sulfinamidines via oxidative amination of sulfenamides using diacetoxyiodobenzene (PhI(OAc)2) and secondary amines under basic conditions. The technique achieves outstanding yields of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27e0cd22c5d3190064bbfe9b3de0bf16
https://doi.org/10.26434/chemrxiv-2023-b0d6x
https://doi.org/10.26434/chemrxiv-2023-b0d6x
Sulfilimines are a class of bioisosteres with immense potential in medicinal chemistry, characterized by the presence of a tetravalent sulfur atom bearing one nitrogen and two distinct carbon substitutes. The conventional methods for synthesizing sul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e9142fb7c397c40be0bf11988eca482
https://doi.org/10.26434/chemrxiv-2023-253pv
https://doi.org/10.26434/chemrxiv-2023-253pv
In this investigation, an unprecedented transition-metal-free and redox-neutral synthesis of sulfilimines was realized through the S-arylation of readily obtainable sulfenamides employing diaryliodonium salts. The pivotal step encompassed the tautome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::011c1b0e04e10e14c6f1c392bdb572a9
https://doi.org/10.26434/chemrxiv-2023-2frs3
https://doi.org/10.26434/chemrxiv-2023-2frs3
Autor:
Guoling Huang
Publikováno v:
2022 IEEE 2nd International Conference on Software Engineering and Artificial Intelligence (SEAI).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab5f7a5d8ca316bf87085ad056383593
https://doi.org/10.1109/seai55746.2022.9832094
https://doi.org/10.1109/seai55746.2022.9832094
Autor:
Peng Zhou, Lu Chen, Shaohua Jiang, Minghua Sun, Jiaming Li, Guoling Huang, Jian Li, Jianrong Li, Yibiao Li, Yubing Huang
Publikováno v:
The Journal of Organic Chemistry. 85:13037-13049
An environmentally sustainable strategy for the chemoselective heterocyclization of bromoenynes through a transition-metal-free sulfuration/cyclization process is reported. Using inexpensive and sa...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c95d35b79d469862c53b3926003b4751
https://doi.org/10.1021/acs.joc.0c01733
https://doi.org/10.1021/acs.joc.0c01733
Autor:
Wenzhe Li, Weijie Dong, Akihiko Kameyama, Guoling Huang, Jianguo Gu, Gang Liu, Zhi Li, Shijie Sun, Yuqing Li
Publikováno v:
Biochemical Journal. 477:1179-1201
Fucosyltransferase 8 (FUT8) and β-galactoside α-2,6-sialyltransferase 1 (ST6GAL1) are glycosyltransferases that catalyze α1,6-fucosylation and α2,6-sialylation, respectively, in the mammalian N-glycosylation pathway. They are aberrantly expressed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cd1137b843f26712866465c9b80dd54
https://doi.org/10.1042/bcj20190789
https://doi.org/10.1042/bcj20190789