Zobrazeno 1 - 10
of 137
pro vyhledávání: '"Dong-Chao Wang"'
Publikováno v:
Organic Letters. 25:3543-3547
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6231f1d969667738ed5eca36e72dfee0
https://doi.org/10.1021/acs.orglett.3c01174
https://doi.org/10.1021/acs.orglett.3c01174
Publikováno v:
The Journal of Organic Chemistry. 87:14284-14298
A Pd/phase-transfer catalyst cooperatively catalyzed domino Heck/allylation reaction is first reported, which represents interesting substrate-dependent regioselectivity. Under the same conditions, Ts-protected
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa6d7bf526fabe89cc6e40cbb668ec63
https://doi.org/10.1021/acs.joc.2c01768
https://doi.org/10.1021/acs.joc.2c01768
Publikováno v:
Organic Chemistry Frontiers. 9:4358-4364
The first catalytic asymmetric route to synthesize chiral thiohydantoins using a chiral phosphoric acid-catalyzed domino cyclization reaction of N,N′-dialkyl thioureas with β,γ-unsaturated α-ketoesters.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7874043cda6b023931b55e2cabf1937c
https://doi.org/10.1039/d2qo00669c
https://doi.org/10.1039/d2qo00669c
Publikováno v:
Organic Letters. 23:7865-7872
A palladium-catalyzed enantioselective Heck cyclization/dearomatization cascade via capturing the cyclized Heck π-allylpalladium intermediate by β-naphthols is reported, which provides a new strategy for the construction of chiral indole-terpenoid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::382e393077b7fca354c57a3ac8d5a665
https://doi.org/10.1021/acs.orglett.1c02881
https://doi.org/10.1021/acs.orglett.1c02881
Publikováno v:
Organic letters. 24(41)
A Ni(II)/bisoxazoline-catalyzed asymmetric dearomative [3+2] cycloaddition of substituted purines with donor-acceptor oxiranes was developed. This reaction, which proceeds via highly chemoselective C-C bond cleavage of the oxiranes, accesses chiral p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80544115f8f12cc91aa2f6f1b8c0133b
https://pubmed.ncbi.nlm.nih.gov/36207146
https://pubmed.ncbi.nlm.nih.gov/36207146
Autor:
Qi-Liang Yang, Ying Liu, Dong-Chao Wang, Tian-Xiang Ren, Gui-Rong Qu, Ming-Sheng Xie, Hai-Ming Guo, Liu-Cheng Guo, Yan-Yan Li
Publikováno v:
Organic Chemistry Frontiers. 8:5410-5417
In this study, an environmentally benign electrochemical protocol for intramolecular oxidative amination is developed, which offers an efficient and sustainable route to access diverse fused tricyclic systems of pyrido[1,2-e]purine-2,4-dione derivati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12af9daff99ce3ec81077d643ae93024
https://doi.org/10.1039/d1qo00959a
https://doi.org/10.1039/d1qo00959a
Palladium-catalyzed asymmetric allylic amination of a vinylethylene carbonate with N-heteroaromatics
Publikováno v:
Organic Chemistry Frontiers. 8:2569-2575
Highly enantioselective allylation of a vinylethylene carbonate by asymmetric palladium catalysis has been developed for a variety of N-heteroaromatic substrates. The employed procedure allows for the efficient synthesis of various acyclic nucleoside
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cda64ffef5b4c2a4401702b60467bd0f
https://doi.org/10.1039/d1qo00272d
https://doi.org/10.1039/d1qo00272d
Publikováno v:
Organic Chemistry Frontiers. 7:1474-1480
Highly enantioselective [5 + 4] annulation of ortho-quinone methides with vinylethylene carbonates has been developed by asymmetric palladium catalysis. The reaction allows for efficient synthesis of various nine-membered benzodioxonines in good yiel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ea78578c15ae76056e6f35abad8a944
https://doi.org/10.1039/d0qo00128g
https://doi.org/10.1039/d0qo00128g
Autor:
jian Song, Yuan Zhu, Xue-Ting Qin, Xue Yang, Lei Wu, Si-Yuan Li, Dong-Chao Wang, Zhi-Hai Wu, MeiYang Yang
Publikováno v:
SSRN Electronic Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20f5c0109664b4bc9af59d47ff81c02b
https://doi.org/10.2139/ssrn.4108412
https://doi.org/10.2139/ssrn.4108412
Publikováno v:
Organic Letters. 22:164-167
A straight synthetic approach to fused polycyclic tropane scaffold formation through an asymmetric dearomatization cycloaddition process of 2-nitrobenzofurans with cyclic azomethine ylides was successfully developed. In the presence of a chiral coppe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::968db99636ab41373abefecff8a738b6
https://doi.org/10.1021/acs.orglett.9b04108
https://doi.org/10.1021/acs.orglett.9b04108