Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Pei-Hao Dou"'
Autor:
Wei-Cheng Yuan, Yong You, Zhen-Hua Wang, Ming-Qiang Zhou, Pei-Hao Dou, Jian-Qiang Zhao, Yan Chen
Publikováno v:
Advanced Synthesis & Catalysis. 363:4047-4053
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d49e5e271c2dd5f6da2a2cd8e6181db
https://doi.org/10.1002/adsc.202100516
https://doi.org/10.1002/adsc.202100516
Autor:
Wen-Ya Lu, Pei-Hao Dou, Xia-Yan Zhang, Zhen-Hua Wang, Wei-Cheng Yuan, Yong You, Jian-Qiang Zhao
Publikováno v:
Chemical Communications. 57:2927-2930
By taking advantage of benzylidene succinimides as a new class of 3C synthons, a highly diastereo- and enantioselective tandem Mannich reaction/transamidation has been established by reacting them with cyclic trifluoromethyl N-acyl ketimines. Using a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b78de7dec92d85a65c57f776d61801fb
https://doi.org/10.1039/d0cc08131k
https://doi.org/10.1039/d0cc08131k
Autor:
Pei-Hao Dou, Shu-Pei Yuan, Yan Chen, Jian-Qiang Zhao, Zhen-Hua Wang, Yong You, Yan-Ping Zhang, Ming-Qiang Zhou, Wei-Cheng Yuan
Publikováno v:
The Journal of organic chemistry. 87(9)
A dearomatization process of 3-nitroindoles enabled using palladium-catalyzed decarboxylative [4 + 2] cycloaddition of either 2-alkylidenetrimethylene carbonates or 2-(hydroxymethyl)-3-arylallyl carbonates has been developed, affording a wide range o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::819b4c1f42ab2ac2fff701c52570f9d8
https://pubmed.ncbi.nlm.nih.gov/35436114
https://pubmed.ncbi.nlm.nih.gov/35436114
Autor:
Shu-Pei Yuan, Pei-Hao Dou, Yun-Qing Jia, Jian-Qiang Zhao, Yong You, Zhen-Hua Wang, Ming-Qiang Zhou, Wei-Cheng Yuan
Publikováno v:
Chemical communications (Cambridge, England). 58(4)
Using 1-thioaurones and 1-azaaurones as electron-deficient oxa-dienes, an organocatalytic asymmetric aromatizing inverse electron-demand [4+2] cycloaddition with γ-deconjugated butenolides and azlactones was developed. A wide range of optically acti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51c623d8187c9d57ca7a8dcf8b45e85f
https://pubmed.ncbi.nlm.nih.gov/34908046
https://pubmed.ncbi.nlm.nih.gov/34908046
Autor:
Xia-Yan, Zhang, Pei-Hao, Dou, Wen-Ya, Lu, Yong, You, Jian-Qiang, Zhao, Zhen-Hua, Wang, Wei-Cheng, Yuan
Publikováno v:
Chemical communications (Cambridge, England). 57(23)
By taking advantage of benzylidene succinimides as a new class of 3C synthons, a highly diastereo- and enantioselective tandem Mannich reaction/transamidation has been established by reacting them with cyclic trifluoromethyl N-acyl ketimines. Using a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6293dfd92247d8f3630d9e5711a4a8f7
https://pubmed.ncbi.nlm.nih.gov/33620365
https://pubmed.ncbi.nlm.nih.gov/33620365
Autor:
Ji-Ya Fu, Jun-Yan Zhu, Chuan-Bao Zhang, Jun Zhang, Qiang-Qiang Wei, Tao Ding, Pei‐Hao Dou, Yan-Bo Wang
Publikováno v:
ChemistrySelect. 1:4403-4407
We have successfully established an efficient catalytic system, which was effective for construction of both spiro[pyrrolidine-benzofuran-3-one] and spiro[pyrrolidine-benzofuran-2-one] compounds. The first 1,3-dipolar cycloaddition of 2-alkylidene-be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50e140ca37a2ae1b0c19a5c4df67e1e1
https://doi.org/10.1002/slct.201600951
https://doi.org/10.1002/slct.201600951
Publikováno v:
Tetrahedron. 76:131116
The first diastereo- and enantioselective cascade Mannich/cyclization reaction of 3-isothiocyanato oxindoles with cyclic ketimines has been successfully developed. By using chiral bifunctional organocatalysts, a range of structurally diverse chiral p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11cdb5a37e14772465d6f7f5bef71fca
https://doi.org/10.1016/j.tet.2020.131116
https://doi.org/10.1016/j.tet.2020.131116
Autor:
Yong Liu, Chuan-Bao Zhang, Ji-Ya Fu, Wei-Qiang Hu, Song-Yang Niu, Pei‐Hao Dou, Zhi-Jun Wu, Yan-Su Cui
Publikováno v:
RSC Advances. 5:70910-70914
The 1,3-dipolar cycloaddition of 2-alkylidene-1-indanone with azomethine ylides has been developed successfully promoted by simple imidazolium salts to construct a variety of spirocycles containing highly substituted pyrrolidines efficiently, affordi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f47fa6250cc6e9ff43a7f34cfabe500
https://doi.org/10.1039/c5ra11536a
https://doi.org/10.1039/c5ra11536a
Autor:
Xiao-Ying Xu, Wei-Cheng Yuan, Yong You, Zhen-Hua Wang, Chuan-Bao Zhang, Ming-Qiang Zhou, Pei-Hao Dou
Publikováno v:
Tetrahedron. 75:130571
An efficient asymmetric [3 + 2]-cycloaddition reaction of 3-isothiocyanato oxindoles and formaldimines in-situ generated from 1,3,5-trisubstituted-hexahydro-1,3,5-triazines with a cinchona alkaloid-derived thiourea as the catalyst has been developed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b8647f6e6275daa167f7715ea202c758
https://doi.org/10.1016/j.tet.2019.130571
https://doi.org/10.1016/j.tet.2019.130571
Autor:
Ji-Ya Fu, Yong Liu, Wei-Qiang Hu, Chuan-Bao Zhang, Pei‐Hao Dou, Yan-Su Cui, Song-Yang Niu, Zhi-Jun Wu
Publikováno v:
ChemInform. 47
The 1,3-dipolar cycloaddition of 2-alkylidene-1-indanone with azomethine ylides has been developed successfully promoted by simple imidazolium salts to construct a variety of spirocycles containing highly substituted pyrrolidines efficiently, affordi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6af19cdf7fc7d4ebb48c7470ec55f0cb
https://doi.org/10.1002/chin.201603096
https://doi.org/10.1002/chin.201603096