Zobrazeno 1 - 10
of 61
pro vyhledávání: '"Jiang-Kai Qiu"'
Autor:
Xin Yuan, Jie Liu, Hao Lv, Long-Zhou Qin, Xiu Duan, Jian Wang, Meng-Yu Wu, Beining Chen, Jiang-Kai Qiu, Kai Guo
Publikováno v:
Green Synthesis and Catalysis, Vol 5, Iss 2, Pp 126-130 (2024)
Photocatalyzed alkylsulfonylation of unactivated alkenes using DABCO. (SO2)2 and thianthrenium salts via a distal heteroaryl migration process has been developed, which provides a new means of synthesizing a variety of valuable alkylsulfonyl-substitu
Externí odkaz:
https://doaj.org/article/7de69996765242439f583c9d7003ab5a
Publikováno v:
Acta Crystallographica Section E, Vol 68, Iss 8, Pp o2325-o2325 (2012)
In the title compound, C11H8F2N2O2·0.5H2O, the dihedral angle between the benzene and isoxazole rings is 8.08 (3)°. In the crystal, the components are linked by O—H...N and N—H...O hydrogen bonds, in which the water molecule acts as both a dono
Externí odkaz:
https://doaj.org/article/7cf0d8a75b824811920439921177c601
Publikováno v:
Acta Crystallographica Section E, Vol 68, Iss 5, Pp o1450-o1450 (2012)
In the title compound, C12H9F3N2O2, the benzene ring is nearly perpendicular to the isoxazole ring, making a dihedral angle of 82.97 (2)°. In the crystal, molecules are linked by N—H...O hydrogen bonds into a supramolecular chain running along the
Externí odkaz:
https://doaj.org/article/344a52e884904dbba777586fb11f9d6c
Publikováno v:
Acta Crystallographica Section E, Vol 68, Iss 5, Pp o1395-o1395 (2012)
In the racemic title compound, C14H17NO6, the plane of the ester group of the methyl hexanoate side chain makes a dihedral angle of 80.0 (2)° with the benzene ring, while the nitro group is approximately coplanar with the benzene ring [dihedral angl
Externí odkaz:
https://doaj.org/article/0d028f4559fc464dbd8278f93cb9161d
Publikováno v:
Acta Crystallographica Section E, Vol 68, Iss 3, Pp o722-o722 (2012)
In the crystal structure of the title compound, C6H7NO2, the molecules are are linked by intermolecular O—H...N and O—H...O hydrogen bonds; π–π stacking is observed between parallel pyridine rings of adjacent molecules [centroid-to-centroid d
Externí odkaz:
https://doaj.org/article/6da82c73fda54b25a11a7facf17de949
Publikováno v:
Advanced Synthesis & Catalysis. 365:555-567
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d36e434585a9ed2d56ce59ec3952f9e6
https://doi.org/10.1002/adsc.202201294
https://doi.org/10.1002/adsc.202201294
Autor:
Shan-Shan Zhu, Ji-Kang Liu, Long-Zhou Qin, Jian Wang, Xiu Duan, Xin Yuan, Jiang-Kai Qiu, Kai Guo
Publikováno v:
The Journal of Organic Chemistry. 88:2057-2068
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2534140a38a80517e833a91c28889f31
https://doi.org/10.1021/acs.joc.2c02336
https://doi.org/10.1021/acs.joc.2c02336
Autor:
Xin Yuan, Jie Liu, Hao Lv, Long-Zhou Qin, Xiu Duan, Jian Wang, Meng-Yu Wu, Beining Chen, Jiang-Kai Qiu, Kai Guo
Publikováno v:
Green Synthesis and Catalysis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78387dea20043e9be8d65556bb3dbfdd
https://doi.org/10.1016/j.gresc.2023.03.002
https://doi.org/10.1016/j.gresc.2023.03.002
Autor:
Qi Sun, Xin‐Peng Zhang, Xiu Duan, Long‐Zhou Qin, Xin Yuan, Meng‐Yu Wu, Jie Liu, Shan‐Shan Zhu, Jiang‐Kai Qiu, Kai Guo
Publikováno v:
Chinese Journal of Chemistry. 40:1537-1545
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e39a5fae23532680c53e5878c9d3f068
https://doi.org/10.1002/cjoc.202200056
https://doi.org/10.1002/cjoc.202200056
Autor:
Xin Yuan, Shengyang Ni, Xiangzhang Tao, Yi Pan, Linyu Kong, Yu Mao, Jiang-Kai Qiu, Yeqing Liu, Yi Wang, Kai Guo
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-7 (2021)
Nature Communications
Nature Communications
Electrosynthesis has received great attention among researchers in both academia and industry as an ideal technique to promote single electron reduction without the use of expensive catalysts. In this work, we report the electrochemical reduction of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2151982541f64ad1aafe56e54ff1d563
https://doaj.org/article/65c1407ac8ad4da8b04cbbba29702ef5
https://doaj.org/article/65c1407ac8ad4da8b04cbbba29702ef5