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- W1567359880 abstract "Publisher Summary This chapter discusses conjugates of calixarenes and heterocycles in the design of newer chemical entities. The various conjugates of calixarenes discussed are: (1) pyridines, piperidine, pyrrolidine and morpholine, (2) quinolines, quinazolines, and phenanthrolines, (3) imidazoles, benzimidazoles, and benzothiazoles, (4) nucleobases, nucleosides, and nucleotides, (5) triazoles, tetrazoles, and triazines, (6) 2,2u-biheterocycles, (7) sugars, and (8) porphyrins and phthalocyanines. This chapter elaborates their design, synthesis, and distinctive features as synthetic receptors. In these conjugates, the heterocyclic components, because of their placement outside the nuclear calixarene frame unlike that in hetero- calixarenes, in addition to their preorganization arising out of the conformational mobility of calixarene platforms, have the added facility of adjustability of the stereochemical and directional dispositions of their binding sites facilitated by their mobility. The utility of the larger size and flexibility of the calixarene hydrophobic cavity has been demonstrated in the designs of metalloenzymes." @default.
- W1567359880 created "2016-06-24" @default.
- W1567359880 creator A5013774277 @default.
- W1567359880 creator A5055055138 @default.
- W1567359880 creator A5091662109 @default.
- W1567359880 date "2009-01-01" @default.
- W1567359880 modified "2023-09-26" @default.
- W1567359880 title "Chapter 4 Conjugates of Calixarenes and Heterocycles in the Design of Newer Chemical Entities" @default.
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