Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Jiao-Zhe Li"'
Autor:
Wen-Ting Wei, Hongxin Liu, Ke-Wei Lei, Yu-Tao Guan, Jiao-Zhe Li, Xue-Er Cai, Sen-Jie Hu, Jun-Hao Zhang
Publikováno v:
Synlett. 33:1917-1924
A novel method for assembling pyrrolidine-2,4-diones from 1,5-enenitriles and acetone/acetonitrile via a cyclization/hydrolysis has been established under metal-catalyst- and base-free conditions, with Oxone as a green oxidant and H2O as an additive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05322a74f63941ac4bd5ee0e1afa0a98
https://doi.org/10.1055/a-1930-7294
https://doi.org/10.1055/a-1930-7294
Autor:
Dong-Kai Wang, Liu-Bin Li, Fa-Liang Liu, Hui Qiu, Jiao-Zhe Li, Jianfeng Zhang, Chao Deng, Wen-Ting Wei
Publikováno v:
ACS Central Science. 8:1028-1034
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c5cf6c82818475b2ae3e92569863ff2
https://doi.org/10.1021/acscentsci.2c00204
https://doi.org/10.1021/acscentsci.2c00204
Autor:
Long Li, Jiao-Zhe Li, Yong-Bin Sun, Chun-Mei Luo, Hui Qiu, Keqi Tang, Hongxin Liu, Wen-Ting Wei
Publikováno v:
Organic Letters. 24:4704-4709
A novel visible-light-catalyzed tandem radical addition/1,5-hydrogen atom transfer/cyclization cascade of 2-alkynylarylethers with sulfonyl chlorides in 2-methyltetrahydrofuran was developed under photocatalyst- and additive-free conditions. This rea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a91455b7eec7547d981c1c4ed371ed6c
https://doi.org/10.1021/acs.orglett.2c01977
https://doi.org/10.1021/acs.orglett.2c01977
Autor:
Jiao‐Zhe Li, Lan Mei, Xue‐Er Cai, Can‐Can Zhang, Ting‐Ting Cao, Xun‐Jie Huang, Yi‐Lin Liu, Wen‐Ting Wei
Publikováno v:
Advanced Synthesis & Catalysis. 364:2080-2085
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4766e5b582c6b14d1d5dc5a5265c6070
https://doi.org/10.1002/adsc.202200272
https://doi.org/10.1002/adsc.202200272
Autor:
Jun-Hao Zhang, Li-Lin Jiang, Sen-Jie Hu, Jiao-Zhe Li, Xuan-Chi Yu, Fa-Liang Liu, Yu-Tao Guan, Ke-Wei Lei, Wen-Ting Wei
Publikováno v:
Organic & Biomolecular Chemistry. 20:7067-7070
The novel polychloromethylation/acyloxylation of 1,6-enynes with chloroalkanes and diacyl peroxides through dual-role designs has been developed to prepare 2-pyrrolidinone derivatives with polychloromethyl units with the use of an inexpensive copper
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98cff92129074b505f7af5b899f839fd
https://doi.org/10.1039/d2ob01330d
https://doi.org/10.1039/d2ob01330d
Publikováno v:
Organic Chemistry Frontiers. 9:5726-5757
C(sp3)–H functionalization is attracting constant attention. This review emphasizes C-centered radicals initiated cyclization strategies by directed C(sp3)–H oxidative functionalization since 2012.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e720f0c1f91c4160b35e0d50b574f86
https://doi.org/10.1039/d2qo01128j
https://doi.org/10.1039/d2qo01128j
Publikováno v:
Organic Chemistry Frontiers. 9:4757-4781
Radical strategies for preparation of seven- or eight-membered rings.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d35441ff12cda5c30af2e61c430c01b7
https://doi.org/10.1039/d2qo00774f
https://doi.org/10.1039/d2qo00774f
Publikováno v:
ChemSusChem. 14:4658-4670
Five-membered N-heterocycles play an important role in organic synthesis and material chemistry, as they are widespread through pharmaceutical molecules and natural products. Chemists have developed many synthetic strategies for constructing five-mem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d93882d2ab7bd74d6de5230fd79e97a0
https://doi.org/10.1002/cssc.202101586
https://doi.org/10.1002/cssc.202101586
Autor:
Wei‐Kang Zhang, Jiao‐Zhe Li, Can‐Can Zhang, Jian Zhang, Yan‐Nan Zheng, Yufang Hu, Ting Li, Wen‐Ting Wei
Publikováno v:
European Journal of Organic Chemistry. 2022
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f61ef784a2d03a5298dd9d48651ff890
https://doi.org/10.1002/ejoc.202200523
https://doi.org/10.1002/ejoc.202200523
Publikováno v:
Organic & Biomolecular Chemistry. 19:7333-7347
The direct use structurally simple ketones as α-ketone radical sources for α-C(sp3)–H functionalization is a sustainable and powerful approach for constructing complex and multifunctional chemical scaffolds with diverse applications. The reaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::38f3b25b8f7643817bae88302ba7c093
https://doi.org/10.1039/d1ob01408k
https://doi.org/10.1039/d1ob01408k