A simple Lewis acid induced reaction of phenols with electrophiles: Synthesis of functionalized 4H-chromenes and ortho-benzylphenols

Sreenivasulu, Chinnabattigalla and Thadathil, Ditto Abraham and Pal, Sumit and G, Satyanarayana (2020) A simple Lewis acid induced reaction of phenols with electrophiles: Synthesis of functionalized 4H-chromenes and ortho-benzylphenols. Synthetic Communications, 50 (1). pp. 112-122. ISSN 0039-7911 (In Press)

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Abstract

Lewis acid ZnCl2 promoted cyclization protocol to 4H-chromenes is accomplished, using readily available phenols and acetophenones as starting materials. Interestingly, the process is feasible under the solvent free environment. Synthesis of a variety of 4H-chromenes have been accomplished using this strategy. In addition, this concept is extended to the synthesis of ortho-benzylphenols by treating phenols either with styrenes or secondary benzylic alcohols.

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IITH Creators:	IITH Creators ORCiD G, Satyanarayana UNSPECIFIED
Item Type:	Article
Uncontrolled Keywords:	4H-chromenes, chalcones, ketones, Lewis acid, phenol, Indexed in Scopus
Subjects:	Chemistry
Divisions:	Department of Chemistry
Depositing User:	Team Library
Date Deposited:	25 Nov 2019 06:48
Last Modified:	25 Nov 2019 06:48
URI:	http://raiithold.iith.ac.in/id/eprint/7055
Publisher URL:	http://doi.org/10.1080/00397911.2019.1689268
Related URLs:	Google Scholar

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