Stereocontrolled synthesis of 1-acetylen-2,3-di-o-benzyl-tetrahydrofurans, 1,4-anhydro-arabinitol, and α,β-dihydroxy-γ-alkyl-butyrolactones (original) (raw)

Stereocontrolled preparation of tetrahydrofurans from acid-promoted rearrangements of allylic acetals

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Journal of The American Chemical Society - J AM CHEM SOC, 1991

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Srinivasan Chandrasekaran

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Srinivasan Chandrasekaran

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Patrick Perlmutter

Tetrahedron Letters, 1995

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General [4 + 1] Cyclization Approach To Access 2,2-Disubstituted Tetrahydrofurans Enabled by Electrophilic Bifunctional Peroxides

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Efficient Synthesis of Furan-2-ylacetates, 7-(Alkoxycarbonyl)benzofurans, and 7-(Alkoxycarbonyl)-2,3-dihydrobenzofurans Based on Cyclization Reactions of Free and Masked Dianions: A “Cyclization/Dehydrogenation” Strategy

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ChemInform Abstract: Dihydroxylation-Based Approach for the Asymmetric Syntheses of Hydroxy-γ-butyrolactones

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Stereospecific formation of tetrahydrofurans from substituted 2,8-Dioxabicyclo[3.2.1]oct-3-ylmethanols

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