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ChemInform Abstract: Boron Trifluoride‐Catalyzed Rearrangement of 2‐Aryloxytetrahydropyrans: A New Entry to C‐Arylglycosidation.

Tadashi Kometani, Hiroyuki Kondo, Yukio Fujimori

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Abstract

Abstract 2‐Aryloxytetrahydropyrans and ‐furans (I) and (IV) rearrange on treatment with boron trifluoride etherate, yielding the 2‐aryl derivatives (II) and (V) as outlined in the reaction scheme.

About this research paper

What this paper is about

Abstract 2‐Aryloxytetrahydropyrans and ‐furans (I) and (IV) rearrange on treatment with boron trifluoride etherate, yielding the 2‐aryl derivatives (II) and (V) as outlined in the reaction scheme.

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Available abstract

Abstract 2‐Aryloxytetrahydropyrans and ‐furans (I) and (IV) rearrange on treatment with boron trifluoride etherate, yielding the 2‐aryl derivatives (II) and (V) as outlined in the reaction scheme.

Key concepts: Boron trifluoride, Chemistry, Catalysis, Boron, Medicinal chemistry, Aryl, Organic chemistry, Alkyl

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ChemInform Abstract: Boron Trifluoride‐Catalyzed Rearrangement of 2‐Aryloxytetrahydropyrans: A New Entry to C‐Arylglycosidation. — Research Paper | ScholarLens