Zobrazeno 1 - 10
of 107
pro vyhledávání: '"Hui-Xiong Dai"'
Autor:
Ming-Liang Han, Jun-Jie Chen, Hui Xu, Zhi-Cong Huang, Wei Huang, Yu-Wen Liu, Xing Wang, Min Liu, Zi-Qiong Guo, Hui-Xiong Dai
Publikováno v:
JACS Au, Vol 1, Iss 11, Pp 1877-1884 (2021)
Externí odkaz:
https://doaj.org/article/0707a59884b44c49902d06e848cd3a7c
Publikováno v:
iScience, Vol 25, Iss 7, Pp 104505- (2022)
Summary: Transition metal-catalyzed C–C bond cleavage is a powerful tool for the reconstruction of a molecular skeleton. We report herein the multi-carbon homologation of aryl ketones to long-chain ketones and aldehydes via ligand-promoted Ar−C(O
Externí odkaz:
https://doaj.org/article/89c8d597e75d4794b9149cc62140042e
Publikováno v:
Chemical Communications. 59:3269-3272
Herein, we report an efficient synthetic method for polysubstituted pentafulvenes via palladium-catalyzed deacetylative [2+2+1] annulation of enones with alkynes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dad82d2310669d6eb94328e2066d26f5
https://doi.org/10.1039/d2cc06644k
https://doi.org/10.1039/d2cc06644k
Publikováno v:
The Journal of Organic Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a06df20ce2d997b2e34974fd587f34e
https://doi.org/10.1021/acs.joc.3c00341
https://doi.org/10.1021/acs.joc.3c00341
Publikováno v:
Synthesis. 54:4727-4733
Spiroindoles are key scaffolds in a large number of natural products, pharmaceuticals, and agrochemicals. Selective C–H activation has emerged as a powerful synthetic approach to streamline the synthesis of substituted spiroindoles. To date, variou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ec455aeb9578ea5666b02f94cc21b85
https://doi.org/10.1055/a-1791-7218
https://doi.org/10.1055/a-1791-7218
Publikováno v:
ACS Catalysis. 12:82-88
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab1dcfa5dbd20d143956f328c445983e
https://doi.org/10.1021/acscatal.1c04010
https://doi.org/10.1021/acscatal.1c04010
Publikováno v:
Organic Letters. 23:8505-8509
We report herein a copper-mediated ortho-C-H amination of anilines using oxalamide as the directing group and DMF as the amination reagent. This protocol tolerates various functional groups and shows good heterocyclic compatibility. Late-stage dimeth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a44b09e74931f051d7ca4c0085ff8fcb
https://doi.org/10.1021/acs.orglett.1c03223
https://doi.org/10.1021/acs.orglett.1c03223
Autor:
Yu-Wen Liu, Ming-Liang Han, Hui-Xiong Dai, Wei Huang, Hui Xu, Min Liu, Xing Wang, Zhi-Cong Huang, Zi-Qiong Guo, Junjie Chen
Publikováno v:
JACS Au, Vol 1, Iss 11, Pp 1877-1884 (2021)
JACS Au
JACS Au
The transition-metal-catalyzed decarboxylation of aryl carboxylic acids has drawn significant attention as an efficient and practical tool for the synthesis of substituted arenes. However, the decarboxylative construction of polysubstituted arenes wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66b1aac17ef5cdadac2ed252885e0cb5
https://doaj.org/article/0707a59884b44c49902d06e848cd3a7c
https://doaj.org/article/0707a59884b44c49902d06e848cd3a7c
Publikováno v:
Chinese Chemical Letters. 32:2765-2768
We report herein a palladium-catalyzed diarylative dearomatization of indole by employing thioester and arylboronic acid as the aryl electrophiles. The reaction involved a decarbonylation/migratory insertion/terminal Suzuki coupling procedure. Substr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8dea3756669c266b5d6dfb0681bc81ad
https://doi.org/10.1016/j.cclet.2021.02.048
https://doi.org/10.1016/j.cclet.2021.02.048
Publikováno v:
Organic letters. 24(40)
Herein, we report an efficient palladium-catalyzed silylation of aryl and alkenyl ketones via C-C bond cleavage and C-Si bond formation. This protocol features high efficiency and broad substrate scope. Further applications in the late-stage diversif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75d3ac5a912519ff523e308d429e4aca
https://pubmed.ncbi.nlm.nih.gov/36178792
https://pubmed.ncbi.nlm.nih.gov/36178792