Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Wen-Kui Yuan"'
Autor:
Lei Wang1, Wen-Kui Yuan1, Zhen-Kai Wang1, Jun Luo1, Tao Zhou1 skybasket@126.com, Bing-Feng Shi1,2,3 bfshi@zju.edu.cn
Publikováno v:
Chinese Journal of Chemistry. Nov2023, Vol. 41 Issue 21, p2788-2792. 5p.
Autor:
Wen-Kui, Yuan, Bing-Feng, Shi
Publikováno v:
Angewandte Chemie (International ed. in English). 60(43)
An unprecedented enantioselective synthesis of spiro-γ-lactams via a sequential C-H olefination/asymmetric [4+1] spirocyclization under a simple Co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3c6402df02d4fc64e3e888b500083466
https://pubmed.ncbi.nlm.nih.gov/34435722
https://pubmed.ncbi.nlm.nih.gov/34435722
Publikováno v:
Organic Chemistry Frontiers. 6:2892-2896
A concise and highly efficient method for the construction of valuable 4-alkynylquinazolines under transition-metal-free conditions was developed via [4 + 2] annulation of 4-alkynylbenzoxazinanones with acylhydroxamates in good to excellent yields. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9e0dcbe35a77d7f75fb5ec0026e5a21
https://doi.org/10.1039/c9qo00668k
https://doi.org/10.1039/c9qo00668k
Publikováno v:
Advanced Synthesis & Catalysis. 359:1373-1378
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9efde9abeafa0603862e7564ddda9d9e
https://doi.org/10.1002/adsc.201601271
https://doi.org/10.1002/adsc.201601271
Publikováno v:
Organic letters. 21(6)
An unprecedented synthesis of valuable benzofuran-3(2 H)-one scaffolds with a quaternary center was developed via Rh/Co relay catalyzed C-H functionalization/annulation of N-aryloxyacetamides with propiolic acids in moderate to good yields. The react
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98453e1598bc1d75f37a60b07da68d0a
https://pubmed.ncbi.nlm.nih.gov/30821152
https://pubmed.ncbi.nlm.nih.gov/30821152
Publikováno v:
Organic letters. 20(22)
An efficient synthesis of thiazolidine-2,4,5-triimine derivatives was developed via Ni-catalyzed oxidative double isocyanide insertion to thioureas under air conditions, in which thioureas play three roles as a substrate, a ligand, and overcoming iso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd60017308016c61c0aa4f6bdac2165a
https://pubmed.ncbi.nlm.nih.gov/30398058
https://pubmed.ncbi.nlm.nih.gov/30398058
Publikováno v:
Organic letters. 20(6)
A new CuI/1,10-phen-catalyzed reaction for the synthesis of 3-ylideneoxindoles from readily available isatins and ethyl isocyanoacetate, in which ethyl isocyanoacetate acts as a latent two-carbon donor like the Wittig reagent, is reported. A tandem p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e27357ac030cb0a4fb258be0b8628328
https://pubmed.ncbi.nlm.nih.gov/29517237
https://pubmed.ncbi.nlm.nih.gov/29517237
Publikováno v:
ChemInform. 47
A concise and direct synthetic strategy for the construction of 2-aryliminochromene skeleton by cascade three-component coupling reaction of arynes, N,S-keteneacetals, and DMF in good yields has been disclosed. The process demonstrates the first exam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0c447ad6553adc9cded1709b51287c4
https://doi.org/10.1002/chin.201648159
https://doi.org/10.1002/chin.201648159
Publikováno v:
The Journal of organic chemistry. 81(14)
A concise and direct synthetic strategy for the construction of 2-aryliminochromene skeleton by cascade three-component coupling reaction of arynes, N,S-keteneacetals, and DMF in good yields has been disclosed. The process demonstrates the first exam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::137d4296bddfca16978b7c123ecc5b71
https://pubmed.ncbi.nlm.nih.gov/27266363
https://pubmed.ncbi.nlm.nih.gov/27266363
Publikováno v:
ChemInform. 46
The mild and efficient procedure affords a series of pharmaceutically interesting title heterocycles bearing a broad spectrum of functionalities and a (Z) configurated side chain.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8fd0c8e2c4d8d2c19c6dfb46413bc9da
https://doi.org/10.1002/chin.201540196
https://doi.org/10.1002/chin.201540196