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Biomimetic Modelling of Organic Synthesis: Studies Involving Cyclodextrins, briefely describes about the cyclodextrins and the structural features of its exterior surface and internal cavity, and its applications in biomimetic synthesis of selenazoles, thiazoles and amino thiazoles; nucleophilic ring opening, oxidative deprotections, substitution and addition reactions in aqeous media. Cyclodextrins are mimicking enzymes in their capability to bind substrates selectively and catalyze chemical reactions through the reversible formation of hostguest complexes by noncovalent bonding. Based on this phenomena, in this work efforts have been made for attaining higher regioselectivities in various ring opening reactions. This work also explores the anionic reactions in aqeous media and in open air atmosphere and contributes greately to the green chemistry by minimising the usage of hazardous organic solvents.
⚠️ WARNING (California Proposition 65):
This product may contain chemicals known to the State of California to cause cancer,
birth defects, or other reproductive harm.
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