2016ChemInformRequires access

ChemInform Abstract: Regioselective Dihydropyran Formation from 4‐Iodo‐2,6‐disubstituted Tetrahydropyran Derivatives Using In(OAc)3/LiI System as the Promoter.

Thibaut Chalopin, Khaoula Jebali, Catherine Gaulon‐Nourry, F. Dénès, Jacques Lebreton, Monique Mathé‐Allainmat

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Abstract

Abstract Starting from 2‐substituted homoallyl alcohols and various aldehydes a diastereomeric mixture of 2,6‐disubstituted 4‐iodotetrahydropyrans is prepared, and the products are further subjected to the regioselective elimination to form dihydropyran derivatives with an ether functionality in position 6.

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What this paper is about

Abstract Starting from 2‐substituted homoallyl alcohols and various aldehydes a diastereomeric mixture of 2,6‐disubstituted 4‐iodotetrahydropyrans is prepared, and the products are further subjected to the regioselective elimination to form dihydropyran derivatives with an ether functionality in position 6.

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Available abstract

Abstract Starting from 2‐substituted homoallyl alcohols and various aldehydes a diastereomeric mixture of 2,6‐disubstituted 4‐iodotetrahydropyrans is prepared, and the products are further subjected to the regioselective elimination to form dihydropyran derivatives with an ether functionality in position 6.

Key concepts: Chemistry, Dihydropyran, Tetrahydropyran, Regioselectivity, Diastereomer, Ether, Organic chemistry, Medicinal chemistry

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ChemInform Abstract: Regioselective Dihydropyran Formation from 4‐Iodo‐2,6‐disubstituted Tetrahydropyran Derivatives Using In(OAc)3/LiI System as the Promoter. — Research Paper | ScholarLens