Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Shaoyu, Mai"'
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-12 (2019)
Alternative carbene precursors for metal-catalyzed cross coupling may expand the portfolio of methods for C-C bond construction. Here, the authors report a Suzuki−Miyaura coupling of Pd−carbene complexes formed by desulfurization of thioureas or
Externí odkaz:
https://doaj.org/article/bfe108ec1527461d8549096d0ce3050f
Publikováno v:
Organic Chemistry Frontiers. 10:2171-2176
An efficient and novel method has been developed for the synthesis of indazole-containing biheteroaryls via a domino Sonogashira coupling/azaenyne cycloisomerization/Barton–Kellogg reaction.
Publikováno v:
International Conference on Cloud Computing, Performance Computing, and Deep Learning (CCPCDL 2023).
Autor:
Zhiqing Zhong, Mingdian Liang, Zhenwei Zhang, Haili Cui, Ningyue Wang, Shaoyu Mai, Huaming Tao
Publikováno v:
Organic Letters. 24:4850-4854
A novel strategy for the synthesis of imidazo-fused polycyclic compounds under mild, base-free, and silver-free conditions by a rhodium(III)-catalyzed C-H annulation of alkenyl or arylimidazoles and (hetero)cyclic 1,3-dicarbonyl compounds is reported
Base-promoted anaerobic intramolecular cyclization synthesis of 4,5-disubstituted-1,2,3-thiadiazoles
Publikováno v:
Organic Chemistry Frontiers. 9:2647-2652
An alkali-promoted, transition-metal-free and oxidant-free method to construct 4,5-disubstituted-1,2,3-thiadiazoles from N-tosylhydrazone-bearing thiocarbamates by employing a sustainable intramolecular reaction strategy has been developed.
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 11, Iss 1, Pp 2158-2165 (2015)
A copper-catalyzed oxidative direct formation of amides from nonactivated carboxylic acids and azoles with dioxygen as an activating reagent is reported. The azole amides were produced in good to excellent yields with a broad substrate scope. The mec
Externí odkaz:
https://doaj.org/article/dd20d6badf664b6fa4c3e0b886e2d4b5
Autor:
Ban Mohammed, Meitao Duan, Shaoyu Mai, Yongyan Zhu, Quanhong Zhu, Ahmed Mahal, Maysoon Al-Haideri, Huaming Tao
Publikováno v:
Natural Product Research. 36:5268-5276
Three new derivatives of tetrahydrocurcumin 6, 7 and 9 have been prepared as potent antitumor agents using copper(II)-catalyzed 'click chemistry'. Their structures were identified using 1H-NMR, 13C-NMR and HRMS techniques. MTT (3-(4,5-dimethylthiazol
Publikováno v:
Organic Letters. 23:3518-3523
Inspired by the body circulation of Omeprazole (irreversible proton pump inhibitor), we disclose the carbene-triggered cascades for the synthesis of 2-aminobenzofuran derivatives from N-sulfonyl-1,2,3-triazoles or benzothioazole-bearing thiocarbamate
Publikováno v:
Organic Letters. 22:7874-7878
An important framework of o-amino benzofuranthioethers was constructed by Cu-catalyzed arylative cyclization of N-tosylhydrazone-bearing thiocarbamates with silylaryl triflates or ArI. This transformation provides a novel strategy for the synthesis o
Publikováno v:
Science Bulletin. 64:1685-1690
Anti-vicinal diboronates were fabricated from easily available diarylethynes and B2pin2 via a base-catalyzed domino-borylation-protodeboronation (DBP) strategy under transition-metal-free conditions. Under the standard conditions, reactants with a ra