Zobrazeno 1 - 10
of 262
pro vyhledávání: '"Guanyinsheng Qiu"'
Autor:
Yangling Deng, Xiya Cheng, Heping Tan, Yuxuan He, Changmei Zhang, Guanyinsheng Qiu, Danqing Zheng
Publikováno v:
Advanced Synthesis & Catalysis. 365:865-870
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e20b67f07f081a0c1f4e29fbb9fc6faf
https://doi.org/10.1002/adsc.202300035
https://doi.org/10.1002/adsc.202300035
Autor:
Ponsiree Jithavech, Pahweenvaj Ratnatilaka Na Bhuket, Wiwat Supasena, Guanyinsheng Qiu, Shengqing Ye, Jie Wu, Tin Wui Wong, Pornchai Rojsitthisak
Publikováno v:
Frontiers in Pharmacology, Vol 11 (2020)
Liver S9 (LS9) is a nearly complete collection of all hepatic drug-metabolizing enzymes. It is a low-cost model for predicting drug metabolic activity. This study aimed to identify the suitability of using LS9 of different animal sources in drug meta
Externí odkaz:
https://doaj.org/article/e8206a17a5124d44adb9594d221772f0
Publikováno v:
Chinese Chemical Letters. 33:4870-4873
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33e2f165dec4f81d0f8de54ad3fb2d73
https://doi.org/10.1016/j.cclet.2022.02.028
https://doi.org/10.1016/j.cclet.2022.02.028
Publikováno v:
Current Chinese Science. 2:400-406
Backgroup: The versatile 2-alkynylbenzamde has been reported to produce many privileged skeletons, like isoquinolin-1-ones, isocoumarin-1-imines, isoindolin-1-ones, and isobenzofuran-1-imines. Recently, we reported the projected transformation using
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de1c5fa556aa57fce4f174c1ac60dcda
https://doi.org/10.2174/2210298102666220524151115
https://doi.org/10.2174/2210298102666220524151115
Autor:
Yuan Zhang, Tongda Liu, Li Liu, Haiyang Guo, Heyang Zeng, Wei Bi, Guanyinsheng Qiu, Wei Gao, Xin Ran, Long Yang, Guanben Du, Lianpeng Zhang
Publikováno v:
The Journal of Organic Chemistry. 87:8515-8524
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2db302ba1da5a654341b9dfc079a59b9
https://doi.org/10.1021/acs.joc.2c00620
https://doi.org/10.1021/acs.joc.2c00620
Autor:
Ming Hou, Zhide Zhang, Xiaojing Lai, Qianshou Zong, Xinpeng Jiang, Meng Guan, Rui Qi, Guanyinsheng Qiu
Publikováno v:
Organic Letters. 24:4114-4118
In this work, the use of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2138aeff99aa5150e7ed3f3979d5b97d
https://doi.org/10.1021/acs.orglett.2c01176
https://doi.org/10.1021/acs.orglett.2c01176
Publikováno v:
Synthesis. 54:3105-3113
A blue LED-promoted dearomative oxo-spirocyclization of N-aryl-N-(2-hydroxyethyl)propiolamides is developed. The reaction works well to provide a series of selenium-containing benzo[b]pyrrolo[2,1-c][1,4]oxazine-3,9-diones with high efficiency and goo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5299e564396dda9a0a2e54e44320956a
https://doi.org/10.1055/a-1775-2910
https://doi.org/10.1055/a-1775-2910
Autor:
Dianpeng Chen, Jianming Li, Xin Wang, Yingying Shan, Keke Huang, Xiaoyang Yan, Guanyinsheng Qiu
Publikováno v:
Organic Chemistry Frontiers. 9:4209-4220
This review summarizes recent advances in the use of isocyanide as “C1N1” synthons in cyclization.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa829492f47935065d85aa1297f1c516
https://doi.org/10.1039/d2qo00753c
https://doi.org/10.1039/d2qo00753c
Publikováno v:
Synthesis.
A reductive coupling reaction of sodium sulfinates for the synthesis of symmetrical/unsymmetrical thiosulfonates is developed. The reaction takes place in the presence of acetyl chloride and Hantzsch ester under mild conditions and exhibits broad fun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70eb10b31139f72001ca948ba5dbbd46
https://doi.org/10.1055/a-2065-5802
https://doi.org/10.1055/a-2065-5802
Autor:
Zhide Zhang, Yangling Deng, Ming Hou, Xiaojing Lai, Meng Guan, Fengzhi Zhang, Rui Qi, Guanyinsheng Qiu
Publikováno v:
Chemical communications (Cambridge, England). 58(98)
In this work, iron/photoredox dual-catalyzed acyl nitrene formation and the use of acyl nitrene in constructing various C–O bonds are reported for the synthesis of phthalides.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5eaeb8d3717eceb0e65a7dca3e32c42a
https://pubmed.ncbi.nlm.nih.gov/36409232
https://pubmed.ncbi.nlm.nih.gov/36409232