Chemistry of “In‐Water” Reactions: Spotlights on Micellar and Phase‐Transfer Catalysis DOI
Tharique N. Ansari, Gaganpreet Kaur, Thomas J. Colacot

и другие.

Опубликована: Ноя. 8, 2024

Custom-designed additives play a crucial role in achieving desired transformations under aqueous conditions modern organic synthesis. In micellar catalysis, designer amphiphilic molecules create dynamic supramolecular structures that can dissolve reactants and catalysts conditions. This enables the to occur mild without need for hazardous solvents. Additionally, such as tetra -butyl ammonium chloride or bromides facilitate reactions through efficient transfer of reactive species between non-miscible biphasic systems. method, known phase-transfer has been instrumental challenging asymmetric chapter overviews recent advancements these respective fields, outlining fundamental principles underlying their operational mechanisms.

Язык: Английский

Aromatic Alcohol-Based pH-Sensitive Chromophore with a Unique Near-Infrared Dual-Band Solvatochromic Property and Its Application as a Ratiometric Fluorescent Sensor for G-Quadruplexes DOI
Bo-Lin Wang,

Pengju Zeng,

Chuang Jiang

и другие.

Analytical Chemistry, Год журнала: 2024, Номер 96(16), С. 6186 - 6194

Опубликована: Апрель 9, 2024

Solvatochromes have gained great attention because of their unique roles in monitoring biomolecular location, interaction, and dynamics. Particularly, solvatochromes presenting both red-shifting excitation dual-band switchable emission are demand yet significantly difficult to come true. In this article, we disclose an aromatic alcohol-based pH-sensitive chromophore NIR-HBT that not only presents solvent-dependent but also shows high photostability excellent brightness. To the best our knowledge, is first solvatochrome simultaneously display these optical properties. Especially, contrast reported whose solvatochromism achieved by affecting excited state behaviors, realized modulating its ground proton dissociation, which a new solvatochromic mechanism has been reported. Furthermore, based on intrinsic binding ability GQs, near-infrared ratiometric detection GQs achieved. These results indicate attractive can be used develop biosensors for biological research. More broadly, discovered open horizons exploring solvatochrome.

Язык: Английский

Процитировано

0

Reversing the Trend: Deciphering Self‐Assembly of Unconventional Amphiphiles Having Both Alkyl‐Chain and PEG DOI
Rita Ghosh,

Bharat Singh,

Subhadip Basu

и другие.

ChemPlusChem, Год журнала: 2024, Номер 89(8)

Опубликована: Апрель 16, 2024

In the field of molecular self-assembly, core an assembly is always made up hydrophobic moiety like a long alkyl chain, whereas outer part has been hydrophilic such as poly(ethylene glycol) (PEG), or charged species. Hence, reversing trend to manifest self-assembled structures with PEG and surface consisting chains in aqueous system incredibly challenging. Herein, we architected unique class cationic bolaamphiphiles containing low weight different lengths. The spontaneously form vesicles without external stimuli. These are unprecedented because makes vesicle core, while appear on vesicles' exterior. this particular design reverses usual self-assembly formation. size increases increase chain-length. To our great surprise, obtained large micelles for longest alkyl-chain amphiphile, which turn act gemini amphiphile. shift from bolaamphiphile amphiphile variation chain also unexplored. Therefore, specific structure would compound new paradigm supramolecular chemistry.

Язык: Английский

Процитировано

0

Micelle Enabled Buchwald‐Hartwig Amination in Water with the Bening by Design Surfactant TPGS‐750‐M for the Synthesis of the JAK Inhibitor 4‐((2‐Chlorophenyl)amino)‐6‐((6‐methylpyridin‐2‐yl)amino)nicotinamide DOI
Hao Jiang, Bin Wu,

Dominik Rufle

и другие.

Helvetica Chimica Acta, Год журнала: 2024, Номер 107(9)

Опубликована: Авг. 11, 2024

Abstract An efficient and scalable Buchwald‐Hartwig amination towards the synthesis of API candidate 4‐((2‐Chlorophenyl)amino)‐6‐((6‐methylpyridin‐2‐yl)amino)nicotinamide as a JAK inhibitor was described. The process developed using water water‐miscible co‐solvent. It facilitated by benign design surfactant TPGS‐750‐M, that promoted robust reliable preparation our target compound in high yields, with improved reaction profile via an operationally simple protocol.

Язык: Английский

Процитировано

0

Chemistry of “In‐Water” Reactions: Spotlights on Micellar and Phase‐Transfer Catalysis DOI
Tharique N. Ansari, Gaganpreet Kaur, Thomas J. Colacot

и другие.

Опубликована: Ноя. 8, 2024

Custom-designed additives play a crucial role in achieving desired transformations under aqueous conditions modern organic synthesis. In micellar catalysis, designer amphiphilic molecules create dynamic supramolecular structures that can dissolve reactants and catalysts conditions. This enables the to occur mild without need for hazardous solvents. Additionally, such as tetra -butyl ammonium chloride or bromides facilitate reactions through efficient transfer of reactive species between non-miscible biphasic systems. method, known phase-transfer has been instrumental challenging asymmetric chapter overviews recent advancements these respective fields, outlining fundamental principles underlying their operational mechanisms.

Язык: Английский

Процитировано

0