Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Guan-Wu Yin"'
Autor:
Xing-Wei Gu, Yu-Li Sun, Jia-Le Xie, Xing-Ben Wang, Zheng Xu, Guan-Wu Yin, Li Li, Ke-Fang Yang, Li-Wen Xu
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-9 (2020)
Catalytic asymmetric hydrosilylation of internal alkenes has proven elusive due to more favourable double bond reduction or isomerization. Here, the authors show an enantioselective Si-C coupling by hydrosilylation of activated alkenes using a pallad
Externí odkaz:
https://doaj.org/article/22450d70f92445818b71e7af0f1e2de3
Autor:
Ren-He Tang, Zheng Xu, Yi-Xue Nie, Xu-Qiong Xiao, Ke-Fang Yang, Jia-Le Xie, Bin Guo, Guan-Wu Yin, Xue-Min Yang, Li-Wen Xu
Publikováno v:
iScience, Vol 23, Iss 7, Pp 101268- (2020)
Summary: Chirality widely exists in a diverse array of biologically active molecules and life forms, and the catalytic constructions of chiral molecules have triggered a heightened interest in the fields of chemistry and materials and pharmaceutical
Externí odkaz:
https://doaj.org/article/8a55fe7771284a8ea78eadcd9e535aab
Publikováno v:
ACS Sustainable Chemistry & Engineering. 10:13133-13144
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3060ae2fbaf4f1d1a8c57e82cfa9d7ce
https://doi.org/10.1021/acssuschemeng.2c03951
https://doi.org/10.1021/acssuschemeng.2c03951
Publikováno v:
Asian Journal of Organic Chemistry. 10:2883-2887
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9bc8b1914b568643c8a1fe2e81024fb6
https://doi.org/10.1002/ajoc.202100502
https://doi.org/10.1002/ajoc.202100502
Autor:
Yi-Xue Nie, Zheng Xu, Jean-Philippe Bouillon, Guan-Wu Yin, Jia-Le Xie, Jian Cao, Han-Qi Zhou, Li-Wen Xu
Publikováno v:
Science China Chemistry. 64:761-769
Hydrosilylation is one of the most important reactions in synthetic chemistry and ranks as a fundamental method to access organosilicon compounds in industrial and academic processes. However, the enantioselective construction of chiral-at-silicon co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59dbccc36aeb1c3b1a5a9d3741133844
https://doi.org/10.1007/s11426-020-9939-1
https://doi.org/10.1007/s11426-020-9939-1
Publikováno v:
Chemical Science. 12:13737-13743
Catalytic asymmetric variants for functional group transformations based on carbon-carbon bond activation still remain elusive. Herein we present an unprecedented palladium-catalyzed (3 + 2) spiro-annulation merging C(sp2)-C(sp2) σ bond activation a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eda8a69daaf6095291098b8910e07874
https://doi.org/10.1039/d1sc04558j
https://doi.org/10.1039/d1sc04558j
Autor:
Guan-Wu Yin, Li Li, Xing-Feng Bai, Jian Cao, Zheng Xu, Yu-Li Sun, Ke-Fang Yang, Li-Wen Xu, Yu-Ming Cui, Jun-Han Ma
Publikováno v:
Science China Chemistry. 63:1082-1090
The catalytic asymmetric synthesis of novel and chiral amino acid derivatives with unconventional chemo-, diastereo-, and enantio-selectivity remains a paramount challenge. Herein we reported a novel protocol for the use of highly enantioselective co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::234e8e87be6ab1b151a6f9dc556a73fc
https://doi.org/10.1007/s11426-020-9768-x
https://doi.org/10.1007/s11426-020-9768-x
Autor:
Xing‐Ben Wang, Zhan‐Jiang Zheng, Jia‐Le Xie, Xing‐Wei Gu, Qiu‐Chao Mu, Guan‐Wu Yin, Fei Ye, Zheng Xu, Li‐Wen Xu
Publikováno v:
Angewandte Chemie. 132:800-807
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1972f4532725be08042fa6d8c59dd05
https://doi.org/10.1002/ange.201913060
https://doi.org/10.1002/ange.201913060
Autor:
Li-Wen Xu, Zhi-Yuan Zhao, Guan-Wu Yin, Zhan-Jiang Zheng, Yi-Xue Nie, Yu-Ming Cui, Ren-He Tang, Zheng Xu, Jian Cao
Publikováno v:
ACS Catalysis. 9:9110-9116
Catalytic hydrosilylation of alkenes ranks as one of the most important academic and industrial synthetic reactions in homogeneous catalysis and organosilicon chemistry. In this work, a highly enan...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b918d3b5d7a96fd0a54b9f475a7f2aa
https://doi.org/10.1021/acscatal.9b02623
https://doi.org/10.1021/acscatal.9b02623
Publikováno v:
Chemical Communications. 55:14363-14366
A unique 1,3-dipolar [3+2] cycloaddition of alkyl 4-oxo-4-arylbut-2-enoates bearing two different electron-withdrawing groups was completed by using the silver/(R)-DTBM-Segphos catalyst system, which gives the corresponding fully substituted pyrrolid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::765d71266319ef7a521555baec524862
https://doi.org/10.1039/c9cc07738c
https://doi.org/10.1039/c9cc07738c