Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Xingliang Nie"'
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-10 (2022)
Sulfonyl fluorides are compounds with potential application in chemical biology and drug discovery, but their preparation can be challenging. Here, the authors present a type of bench-stable fluorosulfonyl radical reagents that enable radical fluoros
Externí odkaz:
https://doaj.org/article/32b1ae80f72a4c1faff125f694b0fc31
Publikováno v:
Organic Chemistry Frontiers. 9:4854-4860
SO2 radical insertion/fluorination via a photocatalytic redox strategy is developed, providing an efficient and reliable approach for the synthesis of alkylsulfonyl fluorides.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d73df065081b4c15632c5f544cea51ab
https://doi.org/10.1039/d2qo00861k
https://doi.org/10.1039/d2qo00861k
Autor:
Xingliang Nie, Saihu Liao
Publikováno v:
Synlett. 33:401-408
Sulfonyl fluorides have widespread applications in many fields. In particular, the increasing research interest on the study of sulfonyl fluorides in the context of chemical biology and drug discovery in the past decade has raised a high demand for n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8244a2fb368f62b970d52a52b90e9472
https://doi.org/10.1055/a-1700-6453
https://doi.org/10.1055/a-1700-6453
Publikováno v:
Angewandte Chemie International Edition. 60:22035-22042
Sulfonyl fluorides have widespread applications in many important fields, including ligation chemistry, chemical biology, and drug discovery. Therefore, new methods to increase the synthetic efficiency and expand the available structures of sulfonyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ad32905105e3efeff0fd8e62199aadc
https://doi.org/10.1002/anie.202109072
https://doi.org/10.1002/anie.202109072
Autor:
Yong Chen, Jinshuai Song, Anandkumar Devaraj, Tianxiao Xu, Saihu Liao, Bolun Zhang, Xingliang Nie
Publikováno v:
Angewandte Chemie International Edition. 60:3956-3960
Sulfonyl fluorides have widespread applications in many fields. In particular, their unique biological activity has drawn considerable research interest in the context of chemical biology and drug discovery in the past years. Therefore, new and effic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::007a596ffa3154513cdd68853e389093
https://doi.org/10.1002/anie.202012229
https://doi.org/10.1002/anie.202012229
Autor:
Peng Wang, Honghai Zhang, Mingqi Zhao, Shuangshuang Ji, Lu Lin, Na Yang, Xingliang Nie, Jinshuai Song, Saihu Liao
Publikováno v:
Angewandte Chemie (International ed. in English). 61(39)
Recently, radical fluorosulfonylation is emerging as an appealing approach for the synthesis of sulfonyl fluorides, which are highly in demand in various disciplines, particularly in chemical biology and drug discovery. Here, we report the first esta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e01a8588534aa73b183317df168da0a
https://pubmed.ncbi.nlm.nih.gov/35943034
https://pubmed.ncbi.nlm.nih.gov/35943034
Autor:
Xingliang Nie, Lin Huang, Zhang Yingyin, Saihu Liao, Qingyuan Feng, Dengfeng Chen, Qiuyue Wang, Yiheng Wang, Shenlin Huang
Publikováno v:
Angewandte Chemie (International ed. in English). 60(52)
Radical fluorosulfonylation is emerging as an appealing approach for the synthesis of sulfonyl fluorides, which have widespread applications in many fields, in particular in the context of chemical biology and drug development. Here, we report the fi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f351d80380e272298421383b8c83794
https://pubmed.ncbi.nlm.nih.gov/34729882
https://pubmed.ncbi.nlm.nih.gov/34729882
Publikováno v:
Organic letters. 22(9)
Thioesters and related thiols are critically important to biological systems and also widely employed in the synthesis of pharmaceutically important molecules and polymeric materials. However, known synthetic methods often suffer from the disadvantag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0b6672cf0f391a0842242d489ebb56b
https://pubmed.ncbi.nlm.nih.gov/32279508
https://pubmed.ncbi.nlm.nih.gov/32279508
Publikováno v:
Tetrahedron Letters. 57:2331-2335
A straightforward, efficient, and highly diastereoselective method for the synthesis of 3,4-cyclopenta-1-tetralones has been realized via the copper-catalyzed coupling of 2-vinyl benzaldehydes with 3-alkenyl 2-bromocarbonyls. Subsequent reduction wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7cdc649af60827bc8c24dd48e837508
https://doi.org/10.1016/j.tetlet.2016.04.069
https://doi.org/10.1016/j.tetlet.2016.04.069
Publikováno v:
Angewandte Chemie (International ed. in English). 56(7)
A palladium-catalyzed three-component reaction between fluoroalkyl bromides, arylboronic acids, and alkenyl aldehydes has been developed and provides facile access to 5-, 6-, or 7-difluoroalkylated ketones under very mild reaction conditions. The res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3dc6dc6e24baaf8959c13c9a31e36831
https://pubmed.ncbi.nlm.nih.gov/28079957
https://pubmed.ncbi.nlm.nih.gov/28079957