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The total synthesis of racemic talatisamine

Pure and Applied Chemistry (1975) 41(1-2) 93-112
DOI: 10.1351/pac197541010093
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Abstract

The first synthesis of a hexacyclic polysubstituted aconite alkaloid with a rearranged skeleton is described. The crucial step of the synthesis is a rearrangement of an atisine-type intermediate. This rearrangement step is related to the assumed biogenesis of delphinine-type alkaloids. © 1975, Walter de Gruyter. All rights reserved.

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APA

Wiesner, K. (1975). The total synthesis of racemic talatisamine. Pure and Applied Chemistry, 41(1–2), 93–112. https://doi.org/10.1351/pac197541010093

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