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A new breakthrough in the synthesis of chiral 3,6-Dihydro-2H-pyrans

Bansal and coworkers have recently succeeded in obtaining a series of phenyl substituted 3,6-Dihydro-2H-pyran derivatives in 68 to 95 percent enantiomeric excess

Bentham Science Publishers

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IMAGE: The pyran ring is present in so many useful compounds. view more

Credit: Bansal et al, Bentham Science Publishers

The pyran ring is present in so many useful compounds, such as pharmaceuticals (antibiotics, anti-infectives, cardiovascular agents, neurological modulators, anti-allergic, anti-asthmatic, anti-inflammatory agents, reproductive and genitourinary agents, growth promoters and antidiabetic agents), veterinary products, agrochemicals, toxins, polymers and additives, photosensitizers and photoinitiators, surfactants, food products, dyes and pigments, This fact keeps motivating synthetic organic chemists to develop newer facile synthetic methods to make these compounds accessible in high enantiomeric purity. Bansal and co-workers have recently succeeded in obtaining a series of phenyl substituted 3,6-Dihydro-2H-pyran derivatives in 68 to 95% enantiomeric excess.

This report has two important features. It illustrates that differently substituted 2-phenyl-3,6-dihydro-2H-pyrans can be obtained in high yield with high enantiomeric purity involving relatively simple experimental method. Secondly, the enantiomeric excess has been rationalized on the basis of computational calculations at the DFT level. It is hoped that the results would be useful for further research in this field.

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Nidhi Sogani, R. K. Bansal and Pragya Sinha

Department of Chemistry, The IIS University, Jaipur, India

This article is open access and can be downloaded from the following link on Bentham Science Publishers' website: http://benthamscience.com/journals/current-catalysis/article/138117/ or http://www.eurekaselect.com/138117/article

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