Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Zhong-Yi Mao"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 795-800 (2019)
A diastereoselective approach to axially chiral imidazopyridine-containing biaryls has been developed. The reactions proceed through a radical cyclization cascade to construct the biaryls with good to excellent central-to-axial chirality transfer.
Externí odkaz:
https://doaj.org/article/4a82068ceba84f54873d907e9b5b7ab6
Publikováno v:
Organic & Biomolecular Chemistry. 19:8789-8793
The development of electrocatalytic synthetic methods hinges on efficient molecular catalysts. Triarylamines are well-known redox catalysts because of the good stability of their corresponding amine radical cations. Herein we show that tris(4-(tert-b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1357a3d8d01ef157ebe95a9d6837cd78
https://doi.org/10.1039/d1ob01644j
https://doi.org/10.1039/d1ob01644j
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 795-800 (2019)
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 795-800 (2019)
A diastereoselective approach to axially chiral imidazopyridine-containing biaryls has been developed. The reactions proceed through a radical cyclization cascade to construct the biaryls with good to excellent central-to-axial chirality transfer.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0ecd78413dee52cfe32b575b3287969
https://doi.org/10.3762/bjoc.15.76
https://doi.org/10.3762/bjoc.15.76
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2018, 20 (13), pp.4057-4061. ⟨10.1021/acs.orglett.8b01616⟩
Organic Letters, American Chemical Society, 2018, 20 (13), pp.4057-4061. ⟨10.1021/acs.orglett.8b01616⟩
International audience; The synthesis of bi- and tricyclic structures incorporating pyrrolidone rings is disclosed, starting from resonance-stabilized acetamides and cyclic α,β-unsaturated-γ-oxycarbonyl derivatives. This process involves an interm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::860382d3bd15577e3681d8eab7e34c67
https://doi.org/10.1021/acs.orglett.8b01616
https://doi.org/10.1021/acs.orglett.8b01616
Autor:
Elisabetta Martini, Zhong-Yi Mao, Pei-Qiang Huang, Giovanni Poli, Julie Oble, Guillaume Prestat
Publikováno v:
Tetrahedron Letters
Tetrahedron Letters, Elsevier, 2017, 58 (44), pp.4174-4178. ⟨10.1016/j.tetlet.2017.09.046⟩
Tetrahedron Letters, 2017, 58 (44), pp.4174-4178. ⟨10.1016/j.tetlet.2017.09.046⟩
Tetrahedron Letters, Elsevier, 2017, 58 (44), pp.4174-4178. ⟨10.1016/j.tetlet.2017.09.046⟩
Tetrahedron Letters, 2017, 58 (44), pp.4174-4178. ⟨10.1016/j.tetlet.2017.09.046⟩
International audience; Pd-catalyzed allylations of cyclic bis-allylic substrates, carried out either as two separate steps or in a pseudo-domino fashion, can generate 2-carboxyl-hexahydroindoles bearing an unsaturation in different positions. Sequen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bc1d0ca6bd3851ab22f5ed07c7984a5
https://doi.org/10.1016/j.tetlet.2017.09.046
https://doi.org/10.1016/j.tetlet.2017.09.046
Publikováno v:
Synlett. 28:1867-1872
The oxidative [3+2] cycloaddition of alkynes with arylamines is a powerful method for the synthesis of (aza)indoles because it employs unfunctionalized and easily available materials. Herein, recent progress in the synthesis of (aza)indoles through t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86287463b36fcccd08badf90b1f938b7
https://doi.org/10.1055/s-0036-1590842
https://doi.org/10.1055/s-0036-1590842
Autor:
Zhong‐Wei Hou, Zhong‐Yi Mao, Huai‐Bo Zhao, Yared Yohannes Melcamu, Xin Lu, Jinshuai Song, Hai‐Chao Xu
Publikováno v:
Angewandte Chemie. 128:9314-9318
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e27cda3693d8fc2181ec89131c74ca1
https://doi.org/10.1002/ange.201602616
https://doi.org/10.1002/ange.201602616
Publikováno v:
Angewandte Chemie International Edition. 55:2226-2229
Oxidative generation of synthetically important amidyl radicals from N-H amides is an appealing and yet challenging task. Previous methods require a stoichiometric amount of a strong oxidant and/or a costly noble-metal catalyst. We report herein the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::380fcaed6e6b8cdb8d73a8762e9c91aa
https://doi.org/10.1002/anie.201510418
https://doi.org/10.1002/anie.201510418
Publikováno v:
Organic Chemistry Frontiers. 3:24-37
The first enantioselective and stereodivergent total syntheses of (−)-isochaetominines A–C and all eight 2,3-cis-stereoisomers of (−)-isochaetominine C, including the natural (+)-14-epi-isochaetominine C, and the proposed structures of (−)-ps
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21286e5ead101e4c9c041cd780a77308
https://doi.org/10.1039/c5qo00298b
https://doi.org/10.1039/c5qo00298b
Publikováno v:
Angewandte Chemie (International ed. in English). 57(6)
We have developed a unified strategy for preparing a variety of imidazo-fused N-heteroaromatic compounds through regiospecific electrochemical (3+2) annulation reaction of heteroarylamines with tethered internal alkynes. The electrosynthesis employs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d317b0396221219a97d63fe8676ca4b
https://pubmed.ncbi.nlm.nih.gov/29266679
https://pubmed.ncbi.nlm.nih.gov/29266679