Stereostructural studies on the 4-hydroxylated annonaceous acetogenins: Synthesis of model butenolides of known relative and absolute configuration involving an intriguing translactonization reaction

Thomas R. Hoye; Paul R. Hanson; Linda E. Hasenwinkel; Elizabeth A. Ramirez; Zhiping Zhuang

doi:10.1016/S0040-4039(00)78427-9

Stereostructural studies on the 4-hydroxylated annonaceous acetogenins: Synthesis of model butenolides of known relative and absolute configuration involving an intriguing translactonization reaction

Thomas R. Hoye
, Paul R. Hanson
, Linda E. Hasenwinkel
, Elizabeth A. Ramirez
, Zhiping Zhuang

Research output: Contribution to journal › Article › peer-review

15 Scopus citations

Abstract

Each diastereomer of model butenolides 3 was synthesized from appropriate antipodes of two propylene oxide molecules. Concomitant translactonization reactions have important stereochemical ramifications.

Original language	English (US)
Pages (from-to)	8525-8528
Number of pages	4
Journal	Tetrahedron Letters
Volume	35
Issue number	46
DOIs	https://doi.org/10.1016/S0040-4039(00)78427-9
State	Published - Nov 14 1994

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10.1016/S0040-4039(00)78427-9

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Hoye, T. R., Hanson, P. R., Hasenwinkel, L. E., Ramirez, E. A., & Zhuang, Z. (1994). Stereostructural studies on the 4-hydroxylated annonaceous acetogenins: Synthesis of model butenolides of known relative and absolute configuration involving an intriguing translactonization reaction. Tetrahedron Letters, 35(46), 8525-8528. https://doi.org/10.1016/S0040-4039(00)78427-9

Stereostructural studies on the 4-hydroxylated annonaceous acetogenins: Synthesis of model butenolides of known relative and absolute configuration involving an intriguing translactonization reaction. / Hoye, Thomas R.; Hanson, Paul R.; Hasenwinkel, Linda E. et al.
In: Tetrahedron Letters, Vol. 35, No. 46, 14.11.1994, p. 8525-8528.

Research output: Contribution to journal › Article › peer-review

Hoye, TR, Hanson, PR, Hasenwinkel, LE, Ramirez, EA & Zhuang, Z 1994, 'Stereostructural studies on the 4-hydroxylated annonaceous acetogenins: Synthesis of model butenolides of known relative and absolute configuration involving an intriguing translactonization reaction', Tetrahedron Letters, vol. 35, no. 46, pp. 8525-8528. https://doi.org/10.1016/S0040-4039(00)78427-9

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abstract = "Each diastereomer of model butenolides 3 was synthesized from appropriate antipodes of two propylene oxide molecules. Concomitant translactonization reactions have important stereochemical ramifications.",

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Stereostructural studies on the 4-hydroxylated annonaceous acetogenins: Synthesis of model butenolides of known relative and absolute configuration involving an intriguing translactonization reaction

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