An efficient and versatile synthesis of the butenolide subunit of 4-hydroxylated annonaceous acetogenins

Thomas R. Hoye; Paul E. Humpal; Jorge I. Jiménez; Michael J. Mayer; Lushi Tan; Zhixiong Ye

doi:10.1016/S0040-4039(00)78332-8

An efficient and versatile synthesis of the butenolide subunit of 4-hydroxylated annonaceous acetogenins

Thomas R. Hoye, Paul E. Humpal, Jorge I. Jiménez, Michael J. Mayer, Lushi Tan, Zhixiong Ye

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Abstract

Title butenolides 2 have been synthesized by an efficient and versatile route that provides access to any stereoisomer by use of individual enantiomers of the precursors 3-butyn-2-ol and terminal epoxides.

Original language	English (US)
Pages (from-to)	7517-7520
Number of pages	4
Journal	Tetrahedron Letters
Volume	35
Issue number	41
DOIs	https://doi.org/10.1016/S0040-4039(00)78332-8
State	Published - Oct 10 1994

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title = "An efficient and versatile synthesis of the butenolide subunit of 4-hydroxylated annonaceous acetogenins",

abstract = "Title butenolides 2 have been synthesized by an efficient and versatile route that provides access to any stereoisomer by use of individual enantiomers of the precursors 3-butyn-2-ol and terminal epoxides.",

author = "Hoye, {Thomas R.} and Humpal, {Paul E.} and Jim{\'e}nez, {Jorge I.} and Mayer, {Michael J.} and Lushi Tan and Zhixiong Ye",

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T1 - An efficient and versatile synthesis of the butenolide subunit of 4-hydroxylated annonaceous acetogenins

AU - Hoye, Thomas R.

AU - Humpal, Paul E.

AU - Jiménez, Jorge I.

AU - Mayer, Michael J.

AU - Tan, Lushi

AU - Ye, Zhixiong

PY - 1994/10/10

Y1 - 1994/10/10

N2 - Title butenolides 2 have been synthesized by an efficient and versatile route that provides access to any stereoisomer by use of individual enantiomers of the precursors 3-butyn-2-ol and terminal epoxides.

AB - Title butenolides 2 have been synthesized by an efficient and versatile route that provides access to any stereoisomer by use of individual enantiomers of the precursors 3-butyn-2-ol and terminal epoxides.

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U2 - 10.1016/S0040-4039(00)78332-8

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M3 - Article

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SN - 0040-4039

VL - 35

SP - 7517

EP - 7520

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 41

ER -

An efficient and versatile synthesis of the butenolide subunit of 4-hydroxylated annonaceous acetogenins

Abstract

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