Regioselective Reduction of 2,3-Epoxy Alcohol Derivatives. An Efficient Route to Enantiomerically Pure 2-Alkanols

DOI: 10.1016/S0040-4039(00)77666-0

Source and publish data:

Tetrahedron Letters p. 33 - 36 (1992)

Update date:2022-09-26

Topics: Enantiomerically pure Reduction Regioselective: Authors:

Chong, J. Michael

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Article abstract of DOI:10.1016/S0040-4039(00)77666-0

Reduction of 2,3-epoxy tosylates with DIBAL-H provides high yields of 2-alkanols. Key words: 2,3-epoxy tosylate; regioselective reduction; enantiomerically pure; 2-alkanol

Full text of DOI:10.1016/S0040-4039(00)77666-0

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Regioselective Reduction of 2,3-Epoxy Alcohol Derivatives. An Efficient Route to Enantiomerically Pure 2-Alkanols

DOI: 10.1016/S0040-4039(00)77666-0

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(00)77666-0

Full text of DOI:10.1016/S0040-4039(00)77666-0

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