Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
Mais filtros

Base de dados
Tipo de documento
Intervalo de ano de publicação
1.
J Org Chem ; 89(11): 7573-7578, 2024 Jun 07.
Artigo em Inglês | MEDLINE | ID: mdl-38781561

RESUMO

The catalytic asymmetric conjugate addition of phosphorus nucleophiles to unsaturated compounds, catalyzed by metallic or nonmetallic catalysts, has been extensively developed. However, the enantioselective transformations involving α,ß-unsaturated carboxylic esters for constructing chiral c-p bonds have been rarely reported, particularly in metal-free processes. In this study, we present a novel metal-free methodology for enantioselective 1,4-addition of diarylphosphine oxides to α,ß-unsaturated carboxylic esters using classical chiral oxazaborolidine catalysts. Remarkably high yields and enantioselectivities were obtained for most of the products. Furthermore, these valuable chiral phosphorus esters serve as crucial intermediates that can be transformed into various derivatives including amides, acids, and alcohols in a single step.

2.
Adv Sci (Weinh) ; 11(7): e2305271, 2024 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-38072676

RESUMO

Catalytic hydrogenation of unsaturated hydrocarbons to alkenes and alkanes using molecular hydrogen is one of the most fundamental transformations in organic synthesis. While methodologies involving transition metals as catalysts in homogeneous and heterogeneous processes have been well developed, metal-free catalytic hydrogenation offers an ideal approach for future chemistry. Herein, the common and inexpensive quaternary ammonium salts are first introduced as catalysts in the catalytic hydrogenation system for the transformations from alkynes or olefins into the corresponding olefins or alkanes. Interestingly, the hydrogenation process of alkynes can be controlled to selectively produce alkenes or alkanes under different conditions. Moreover, the possible mechanism is discussed in new insights into the catalytic behavior of quaternary ammonium salts.

3.
Dalton Trans ; 51(9): 3760, 2022 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-35171183

RESUMO

Correction for 'Naphthalimide-containing coordination polymer with mechanoresponsive luminescence and excellent metal ion sensing properties' by Jian-Jun Liu et al., Dalton Trans., 2020, 49, 3174-3180, DOI: 10.1039/C9DT04928B.

4.
Dalton Trans ; 49(10): 3174-3180, 2020 Mar 09.
Artigo em Inglês | MEDLINE | ID: mdl-32091051

RESUMO

Mechanoresponsive luminescent materials coupled with other functionalities are of particular interest due to their multiple external stimuli responsive properties. In this paper, a new sensitive mechanoresponsive luminescent coordination polymer, [Cd(INI)(DMF)2·DMF] (1) (H2INI = N-(5-isophthalic acid)-1,8-naphthalimide), has been successfully designed and synthesized. Complex 1 exhibits interesting mechanoresponsive and grinding-enhanced luminescence properties, and its luminescence colour changed from weak blue-green to bright blue upon grinding owing to the external pressure-induced destruction of ππ stacked arrangements in local defective areas. Moreover, the luminescence properties and uncoordinated carbonyl groups of well-ground g-1 endow it with excellent sensing ability for Cr3+ ions. This work will provide a new perspective to rationally design multifunctional coordination polymers that can serve as practical multi-responsive sensors to pressure and chemicals.

SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA