Issue 43, 2021

Name reactions: strategies in the design of chemodosimeters for analyte detection

Abstract

The design and synthesis of suitable chemodosimeters for the detection of toxic analytes has become challenging for new researchers nowadays in the molecular recognition field. Among different chemical reactions, name reaction-based approaches will help researchers to gain knowledge about different types of name reactions for different analytes, the mechanism of sensing using these reactions, the names of scientists who pioneered these name reactions, and also to explore unknown name reactions for unexplored analytes. In this context, we have reported different sensing strategies, i.e., name reaction-based approaches involved in designing various chemodosimeters during the past decades. The name reaction-based approaches have been classified into 11 types, such as (a) Tsuji–Trost allylic cleavage, (b) Suzuki–Miyaura coupling, (c) Claisen rearrangement, (d) benzil-cyanide reaction, (e) intramolecular crossed-benzoin reaction, (f) Michael addition reaction, (g) Gabriel mechanism, (h) 2-aza-Cope rearrangement, (i) Baeyer–Villiger reaction, (j) Beckmannn rearrangement, and (k) Lossen rearrangement. The focus of the review is mainly on how name reactions are used in analyte detection chemodosimetrically.

Graphical abstract: Name reactions: strategies in the design of chemodosimeters for analyte detection

Article information

Article type
Perspective
Submitted
24 ago 2021
Accepted
01 out 2021
First published
02 out 2021

New J. Chem., 2021,45, 20046-20074

Name reactions: strategies in the design of chemodosimeters for analyte detection

A. Maiti, S. K. Manna, D. Banik and A. K. Mahapatra, New J. Chem., 2021, 45, 20046 DOI: 10.1039/D1NJ04056A

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