An Efficient and Versatile Synthesis of the Butenolide Subunit of 4-Hydroxylated Annonaceous Acetogenins

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

Source and publish data:

Tetrahedron Letters p. 7517 - 7520 (1994)

Update date:2022-09-26

Topics:

Authors:

Hoye, Thomas R.

Humpal, Paul E.

Jimenez, Jorge I.

Mayer, Michael J.

Tan, Lushi

Ye, Zhixiong

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Article abstract of DOI:10.1016/S0040-4039(00)78332-8

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.

Full text of DOI:10.1016/S0040-4039(00)78332-8

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Product name:2-(tert-Butyl-dimethyl-silanyloxy)-15-(4-methoxy-benzyloxy)-pentadec-3-yn-6-ol

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