Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Ruiwen Jin"'
Publikováno v:
Chemical Communications. 56:11621-11624
Light-enabled, AlCl3-catalyzed regioselective intramolecular nucleophilic cyclization of alkynes using non-nucleophilic alkyls as the nucleophile is reported. Upon photoexcitation, o-alkylphenyl alkynyl ketones can be transferred into (E)-photoenols.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d50b78440c9b07c808db8c59f299e11a
https://doi.org/10.1039/d0cc04636a
https://doi.org/10.1039/d0cc04636a
Publikováno v:
Chemical communications (Cambridge, England). 56(78)
Light-enabled, AlCl3-catalyzed regioselective intramolecular nucleophilic cyclization of alkynes using non-nucleophilic alkyls as the nucleophile is reported. Upon photoexcitation, o-alkylphenyl alkynyl ketones can be transferred into (E)-photoenols.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::539612d68930b2c4cf23223a19bec085
https://pubmed.ncbi.nlm.nih.gov/32870204
https://pubmed.ncbi.nlm.nih.gov/32870204
Publikováno v:
Organic letters. 22(14)
This research successfully achieved a Cu(II)-catalyzed 6π-photocyclization of non-6π substrates. The photoenolization converts ortho-alkylphenyl alkynl ketones into a triene-type intermediate which undergoes the subsequent 6π-photocyclization to g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a40b7fbe382aa3528d48849b4a3146a9
https://pubmed.ncbi.nlm.nih.gov/32584588
https://pubmed.ncbi.nlm.nih.gov/32584588
Publikováno v:
Tetrahedron Letters. 59:3880-3883
We report herein a visible light-induced oxidation of triarylphosphines under aerobic condition with excellent functional group tolerance. In this transformation, the photo catalyst 4-phenylthioxanthone acted as a photosensitizer for the in situ gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d068ce49a38cc2ba228b44b4b98b2672
https://doi.org/10.1016/j.tetlet.2018.09.031
https://doi.org/10.1016/j.tetlet.2018.09.031
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-7 (2017)
Scientific Reports
Scientific Reports
In this work, we developed a new method for the transformation of organostannanes via radical process. In this reaction, highly reactive carbon radical species can be efficiently generated through HBr-catalyzed photocleavage of C-Sn bond via single e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2fff1a13f8ddf31cf0f857f27fc500a
http://link.springer.com/article/10.1038/s41598-017-16806-3
http://link.springer.com/article/10.1038/s41598-017-16806-3
Publikováno v:
Synlett. 28:2159-2162
Herein, we wish to report the main-group metal Lewis acid catalyzed intramolecular hydroarylation of arenes with alkynes. This cyclization proceeds efficiently in the presence of a catalytic amount of AlCl3, affording phenanthrenes in moderate to exc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9939f4c568159984c4832db8180623c
https://doi.org/10.1055/s-0036-1588479
https://doi.org/10.1055/s-0036-1588479
Autor:
Dawen Xu, Ruiwen Jin, Aishun Ding, Wangsheng Liu, Yawei Li, Yiyong Chen, Hao Guo, Jinjin Chen
Publikováno v:
The Journal of Organic Chemistry. 81:12553-12558
The first 6π-photocyclization of dienynes was developed, which provides a new and effective protocol for the synthesis of the phenyl ring in excellent yields with nice functional group tolerance. In this transformation, the Cu(OTf)2 catalyst plays a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::479d25381bc14f22320d5e71eb58bd84
https://doi.org/10.1021/acs.joc.6b02537
https://doi.org/10.1021/acs.joc.6b02537
Publikováno v:
Tetrahedron Letters. 57:3235-3238
A Nd(OTf) 3 -catalyzed alkyne-hydroarylation with arenes is reported. This reaction shows a wide range of functional group tolerance. Such a catalytic methodology enriches lanthanide element chemistry and provides a new route for synthesizing phenant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a754c3b8dffdc18a4b81bb2ac7b3750c
https://doi.org/10.1016/j.tetlet.2016.06.053
https://doi.org/10.1016/j.tetlet.2016.06.053
Autor:
Dawen Xu, Ruiwen Jin, Yawei Li, Jinjin Chen, Guangxin Gu, Wangsheng Liu, Yunyan Kuang, Hao Guo, Feifei Ba
Publikováno v:
Organic Chemistry Frontiers. 3:852-855
A CuBr2-promoted cyclization and bromination of arene–alkyne substrates has been developed, affording 9-bromophenanthrene derivatives highly efficiently. This reaction provides a novel and efficient protocol for C–Br bond formation from an inorga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::667b6519d80329ddb72495e79478f930
https://doi.org/10.1039/c6qo00117c
https://doi.org/10.1039/c6qo00117c
Publikováno v:
Chemical Communications. 52:9909-9912
Here, we demonstrate that merging photoredox catalysis with Lewis acid catalysis provides a fundamentally new activation mode of C-C triple bonds, to achieve the bond-forming reaction of alkynes with weak nucleophiles. Using a synergistic merger of E
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a94ff70aff2a5261b9a86cc66ad389c
https://doi.org/10.1039/c6cc03725a
https://doi.org/10.1039/c6cc03725a