A stereodivergent synthesis of (±)-cyclophellitol and (1R,6S)-cyclophellitol from the 7-oxabicyclo-[2.2.1]hept-5-ene-2-endo-carboxylic acid

DOI: 10.1016/0040-4039(96)00464-9

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Tetrahedron Letters p. 3043 - 3044 (1996)

Update date:2022-08-04

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Authors:

Acena Acena

De Alba De Alba

Arjona Arjona

Plumet Plumet

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Article abstract of DOI:10.1016/0040-4039(96)00464-9

A concise, stereodivergent synthesis of (±)-cyclophellitol 1 and its unnatural diastereoisomer (1R*,6S*)-cyclophellitol 2 starting from the Diels-Alder adduct of furan and acrylic acid is reported. The stereochemistry of the key step (the epoxidation of a

Full text of DOI:10.1016/0040-4039(96)00464-9

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Article Doi

A stereodivergent synthesis of (±)-cyclophellitol and (1R*,6S*)-cyclophellitol from the 7-oxabicyclo-[2.2.1]hept-5-ene-2-endo-carboxylic acid

DOI: 10.1016/0040-4039(96)00464-9

Source and publish data: