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1.
Chemistry ; : e202304234, 2024 Apr 21.
Article in English | MEDLINE | ID: mdl-38644695

ABSTRACT

With both TEMPO and O2 (in air) as the homogeneous redox mediators, BiBrO as the heterogeneous semiconductor photocatalyst, the first example of semi-heterogeneous photocatalytic decarboxylative phosphorylation of N-arylglycines with diarylphosphine oxides was established. A series of α-amino phosphinoxides were efficiently synthesized.

2.
Chem Commun (Camb) ; 59(94): 14029-14032, 2023 Nov 23.
Article in English | MEDLINE | ID: mdl-37964611

ABSTRACT

With both ferrocene and air as the redox catalysts, for the first time, the low-cost natural ilmenite (FeTiO3) was successfully used for photocatalytic bond formations. Under the assistance of a traceless H-bond, and HCHO as the methylene reagent, a variety of imidazo[1,5-a]quinoxalinones were semi-heterogeneously photosynthesized in high yields with good functional group compatibility.

3.
Org Biomol Chem ; 21(2): 370-374, 2023 01 04.
Article in English | MEDLINE | ID: mdl-36515252

ABSTRACT

A concise and efficient ring-opening difluorination strategy was developed for the synthesis of highly functionalized hydroxy-containing α,α-difluoro-ß-ketoamides from the one-pot multicomponent reaction of 4-aminocoumarins, NFSI, and water in dimethyl carbonate (DMC) as a green solvent. The reactions were smoothly achieved under visible light irradiation in air at room temperature without the addition of any other external photocatalysts. With this protocol, various α,α-difluoro-ß-ketoamides were successfully synthesized under mild conditions (25 examples, 73-91% yields). This transition-metal-free synthetic procedure shows good functional group compatibility and attractive practical potential for large-scale synthesis.


Subject(s)
Amides , Light , Solvents
4.
Chem Asian J ; 17(1): e202101139, 2022 Jan 03.
Article in English | MEDLINE | ID: mdl-34837338

ABSTRACT

With eco-friendly and sustainable CO2 -derived dimethyl carbonate as the sole solvent, the visible-light-induced cascade radical reactions have been established as a green and efficient tool for constructing various CHF2 /CClF2 /CBrF2 -substituted ring-fused quinazolinones.

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