Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Jianglian Li"'
Autor:
Maoyao He, Yuncan Chen, Yi Luo, Jianglian Li, Ruizhi Lai, Zengbao Yang, Yuerong Wang, Yong Wu
Publikováno v:
Green Synthesis and Catalysis, Vol 1, Iss 2, Pp 180-182 (2020)
An efficient and practical synthetic approach was developed for the tandem synthesis of trisubstituted 2-pyrone derivatives from sulfoxonium ylides and cyclopropenones. This [3+3] annulation reaction was carried out under transition-metal-free condit
Externí odkaz:
https://doaj.org/article/1071a10e4ddf4b54b22baf51cce54e25
Publikováno v:
Synthesis. 54:3015-3024
An iridium-catalyzed reaction protocol has been developed to achieve the oxidative C–H/N–H annulation of benzamides with cyclopropanols as C1 synthon. Structurally diverse isoindolin-1-ones were furnished via sequential C–H/C–C cleavage and C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::150b6a7a27559f57698ff7077541cdde
https://doi.org/10.1055/a-1780-1935
https://doi.org/10.1055/a-1780-1935
Publikováno v:
Chinese Chemical Letters. 32:3984-3987
Carbene transfer reactions play an important role in the field of organic synthesis because of their ability to construct a variety of molecules. Herein, we reported on blue light-induced cyclopropenizations of N-tosylhydrazones in water, which avoid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14fb353f7e7104d750830b9a4ea53a0b
https://doi.org/10.1016/j.cclet.2021.05.031
https://doi.org/10.1016/j.cclet.2021.05.031
Autor:
Yingying Xu, Zhongzhen Yang, Qiantao Wang, Jianglian Li, Yong Wu, Xin Huang, Yi Luo, Ruizhi Lai
Publikováno v:
Chinese Chemical Letters. 32:3518-3521
A new strategy is developed for the synthesis of 1-aminoisoquinoline derivatives. This Rh(III)-catalyzed [4 + 2] annulation reaction employs benzamidines as efficient directing groups and the vinylene carbonate as an acetylene surrogate. Additionally
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b2c6bfc2c6d7bafdf832632e698d39a
https://doi.org/10.1016/j.cclet.2021.04.058
https://doi.org/10.1016/j.cclet.2021.04.058
Publikováno v:
European Journal of Organic Chemistry. 2022
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::668f68b625f4308156ef5d83872c4326
https://doi.org/10.1002/ejoc.202200961
https://doi.org/10.1002/ejoc.202200961
Publikováno v:
Synlett. 32:1963-1968
In the report, we described the ruthenium(II)-catalyzed C–H activation/cyclization of 2-arylquinazolinones with vinyl carbonate for the synthesis of different fused quinazolinones. Through this strategy, the 6-hydroxy-5,6-dihydro-8H-isoquinolino[1,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9789bf091a2289f25a4345accddf807
https://doi.org/10.1055/a-1608-5381
https://doi.org/10.1055/a-1608-5381
Publikováno v:
Synthesis. 54:779-787
A novel ruthenium-catalyzed alkylation of cyclopropanols with sulfoxonium ylides has been developed that affords diverse 1,5-diketones with good efficiency and broad substrate scope. To illustrate the synthetic applications of the obtained 1,5-diketo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f15670834f785172bce815eb7917141a
https://doi.org/10.1055/a-1588-0974
https://doi.org/10.1055/a-1588-0974
Publikováno v:
Chinese Chemical Letters. 32:2555-2558
Sulfoxonium ylides as carbene precursors couple smoothly with thioureas in the presence of 5 mol% of rhodium(II) acetate dimmer via carbenoid insertion to afford the corresponding 2-aminothiazoles with high chemoselectivity, providing a facile and ef
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1dd8e8abc5008cbcfbaedc3b3510480b
https://doi.org/10.1016/j.cclet.2021.02.052
https://doi.org/10.1016/j.cclet.2021.02.052
Publikováno v:
Asian Journal of Organic Chemistry. 10:1683-1686
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f381da97dd4186c64b277ad4cb09079f
https://doi.org/10.1002/ajoc.202100254
https://doi.org/10.1002/ajoc.202100254
Publikováno v:
ChemistrySelect. 5:8562-8565
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d02dcb98a296ca35fc4cace86678a5b0
https://doi.org/10.1002/slct.202002188
https://doi.org/10.1002/slct.202002188