STEREOELECTRONIC FACTORS IN THE SYNTHESIS OF TETRAHYDROFURANS BY HYDROXYL PARTICIPATION IN PHENYLTHIO MIGRATION

DOI: 10.1016/S0040-4039(00)97421-5

Source and publish data:

Tetrahedron Letters p. 3457 - 3460 (1990)

Update date:2022-09-26

Topics: Synthesis Molecular structure Tetrahydrofurans Substrate Experimental nucleophilic stereoelectronic factors

Authors:

McIntyre, Sara

Warren, Stuart

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Article abstract of DOI:10.1016/S0040-4039(00)97421-5

The factors controlling the title reaction were investigated with two tethered hydroxyl nucleophiles and include preferential attack at the more highly substituted carbon atom, preferential formation of the more highly substituted five-membered ring, and

Full text of DOI:10.1016/S0040-4039(00)97421-5

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