A TOTAL SYNTHESIS OF (-)-REISWIGIN A VIA SEQUENTIAL CLAISEN REARRANGEMENT-INTRAMOLECULAR ESTER ENOLATE ALKYLATION

DOI: 10.1016/0040-4039(94)80021-9

Source and publish data:

Tetrahedron Letters p. 7957 - 7960 (1994)

Update date:2022-08-03

Topics:

Authors:

Kim, Deukjoon

Shin, Kye Jung

Kim, Ik Yoen

Park, Sang Woo

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Article abstract of DOI:10.1016/0040-4039(94)80021-9

(-)-Reiswigin A (1), a novel anti-viral diterpene, has been synthesized in a highly stereoselective manner utilizing a sequential Claisen rearrangement intramolecular ester enolate alkylation strategy.

Full text of DOI:10.1016/0040-4039(94)80021-9

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