Total Synthesis of Zoanthamine Alkaloids, Part 2. Construction
                of the C1-C5, C6-C10 and C11-C24 Fragments of Zoanthamine

David Ackland Tanner; Lars Tedenborg; Peter Somfai

Total Synthesis of Zoanthamine Alkaloids, Part 2. Construction of the C1-C5, C6-C10 and C11-C24 Fragments of Zoanthamine

David Ackland Tanner, Lars Tedenborg, Peter Somfai

Research output: Contribution to journal › Journal article › Research › peer-review

Abstract

This paper describes the construction of three key intermediates for a projected total synthesis of the marine alkaloid zoanthamine. These building blocks, corresponding to the C1-C5, C6-C10 and C11-C24 fragments of the target molecule, are synthesised efficiently form (R)-hydroxymethyl-butyrolactone, methyl propiolate, and (S)-prillyl alcohol, respectively.

Original language	English
Journal	Acta Chem. Scand.
Volume	51
Pages (from-to)	1217-1223
Publication status	Published - 1997

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title = "Total Synthesis of Zoanthamine Alkaloids, Part 2. Construction of the C1-C5, C6-C10 and C11-C24 Fragments of Zoanthamine",

abstract = "This paper describes the construction of three key intermediates for a projected total synthesis of the marine alkaloid zoanthamine. These building blocks, corresponding to the C1-C5, C6-C10 and C11-C24 fragments of the target molecule, are synthesised efficiently form (R)-hydroxymethyl-butyrolactone, methyl propiolate, and (S)-prillyl alcohol, respectively.",

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AU - Tanner, David Ackland

AU - Tedenborg, Lars

AU - Somfai, Peter

PY - 1997

Y1 - 1997

N2 - This paper describes the construction of three key intermediates for a projected total synthesis of the marine alkaloid zoanthamine. These building blocks, corresponding to the C1-C5, C6-C10 and C11-C24 fragments of the target molecule, are synthesised efficiently form (R)-hydroxymethyl-butyrolactone, methyl propiolate, and (S)-prillyl alcohol, respectively.

AB - This paper describes the construction of three key intermediates for a projected total synthesis of the marine alkaloid zoanthamine. These building blocks, corresponding to the C1-C5, C6-C10 and C11-C24 fragments of the target molecule, are synthesised efficiently form (R)-hydroxymethyl-butyrolactone, methyl propiolate, and (S)-prillyl alcohol, respectively.

M3 - Journal article

VL - 51

SP - 1217

EP - 1223

JO - Acta Chem. Scand.

JF - Acta Chem. Scand.

ER -