Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Weihao Rao"'
Publikováno v:
Industrial & Engineering Chemistry Research. 60:9296-9303
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4df2e3b063d2c6520ae6747e66385c6
https://doi.org/10.1021/acs.iecr.1c01287
https://doi.org/10.1021/acs.iecr.1c01287
Autor:
Zhen Yang, Lin Tang, Hao Cheng, Weihao Rao, Qiuju Zhou, Hanfei Chen, Shuaifei Zhang, Fang Yang
Publikováno v:
Organic Letters. 23:519-524
A simple and practical photochemical strategy for intermolecular perfluoroalkyl-alkenylation of alkenes with 2-amino-1,4-naphthoquinones and perfluoroalkyl iodides has been demonstrated under visible-light irradiation. Mechanistic studies reveal that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0692ba3aab1282a7c8ea21a55ccd5d31
https://doi.org/10.1021/acs.orglett.0c04036
https://doi.org/10.1021/acs.orglett.0c04036
Autor:
Geng Zhao, Yu-Qiang Zhou, Xiantao Ma, Weihao Rao, Zhen Yang, Guo-Dong Zou, Xueping Chang, Lin Tang
Publikováno v:
Tetrahedron Letters. 59:4272-4275
A convenient and precise nitration and oximation of alkenes with tert-butyl nitrite has been reported, yielding α-nitro ketoximes in satisfactory yields with broad substrate generality and excellent stereoselectivity under mild conditions. Experimen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::638a6c383885c5391709432a990fc4ab
https://doi.org/10.1016/j.tetlet.2018.10.037
https://doi.org/10.1016/j.tetlet.2018.10.037
Autor:
Xiantao Ma, Jingchao Jiao, Lingyun Zheng, Weihao Rao, Xueping Chang, Lin Tang, Zhen Yang, Qiuju Zhou
Publikováno v:
Organic Letters. 20:6520-6525
A practical and efficient method for selective intramolecular radical trifluoromethylacylation and -arylation of alkenes with inexpensive CF3SO2Na and K2S2O8 in aqueous media has been developed, respectively, affording the highly chemoselective synth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f873f973e8df2a772cd2de39982a4cb0
https://doi.org/10.1021/acs.orglett.8b02846
https://doi.org/10.1021/acs.orglett.8b02846
Publikováno v:
Organic Letters. 20:6198-6201
A selective O-cyclization of N-methoxy aryl amides with CH2Br2 or 1,2-DCE (1,2-dichloroethane) via palladium-catalyzed C–H activation has been described. New C(sp3)–O and C(sp2)–C(sp3) bonds are forged simultaneously with the assistance of an N
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9b67efc04680d176423259702068e1ba
https://doi.org/10.1021/acs.orglett.8b02678
https://doi.org/10.1021/acs.orglett.8b02678
Publikováno v:
Advanced Synthesis & Catalysis. 360:3055-3062
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a4a07f8e7d43a562f3b50a3c9ff4a404
https://doi.org/10.1002/adsc.201800586
https://doi.org/10.1002/adsc.201800586
Autor:
Qiuju Zhou, Zhen Yang, Yuqiang Zhou, Jingchao Jiao, Guo-Dong Zou, Weihao Rao, Lin Tang, Ying Cui, Xiantao Ma
Publikováno v:
The Journal of organic chemistry. 84(16)
By altering the amount of Selectfluor, the highly selective mono- and difluorination of 1,3-dicarbonyl compounds has been achieved, affording a variety of 2-fluoro- and 2,2-difluoro-1,3-dicarbonyl compounds in good to excellent yields. The reaction c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::687b6d9f5c8dbcb90ff0ff78838b3b28
https://pubmed.ncbi.nlm.nih.gov/31335142
https://pubmed.ncbi.nlm.nih.gov/31335142
Autor:
Liu Xiaomeng, Lin Tang, Guo-Dong Zou, Jin-Xiao Zhao, Jiang Xin, Yu-Qiang Zhou, Li-Li Jiang, Fang-Yuan Chen, Mei-Jun Chen, Weihao Rao
Publikováno v:
Organic letters. 21(8)
A copper-catalyzed direct aminosulfonylation of unactivated alkenes with sodium sulfinates for the efficient synthesis of sulfonylated pyrrolidones is described. This reaction features good functional group tolerance and wide substrate scope, providi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94a0cfbf1f4d9f8201f8d55d0bc05add
https://pubmed.ncbi.nlm.nih.gov/30958680
https://pubmed.ncbi.nlm.nih.gov/30958680
Autor:
Jia-Jia Chen, Lin Tang, Fang-Yuan Chen, Guo-Dong Zou, Yi-Yuan Guo, Li-Li Jiang, Ying Cui, Weihao Rao, Meng Zhang
Publikováno v:
Tetrahedron Letters. 61:151540
A simple and efficient copper-catalyzed aminooxygenation of unactivated alkenes with commercially available (2,2,6,6-tetramethylpiperidin-1-yl)-oxyl (TEMPO) as an oxygen source is reported. With this protocol, a variety of functionalized pyrrolidones
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08b444b6655d032347caa551b47a4f79
https://doi.org/10.1016/j.tetlet.2019.151540
https://doi.org/10.1016/j.tetlet.2019.151540
Publikováno v:
Angewandte Chemie. 125:13833-13837
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5d4a119d82de075ae1c13ca5a286776
https://doi.org/10.1002/ange.201306625
https://doi.org/10.1002/ange.201306625