STEREOSELECTIVE APPROACH TO TRISUBSTITUTED TETRAHYDROFURANS

DOI: 10.1016/S0040-4039(00)73723-3

Source and publish data:

Tetrahedron Letters p. 6251 - 6254 (1993)

Update date:2022-08-04

Topics:: Authors:

Mohr, Peter

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Article abstract of DOI:10.1016/S0040-4039(00)73723-3

Functionalized allylsilanes 1 undergo with acetals 2 under mild Broensted acid catalysis a transacetalization-ring closure reaction to afford in fair to good yield and high diastereoselectivity all-cis-tetrahydrofurans 3.The stereochemical outcome is inde

Full text of DOI:10.1016/S0040-4039(00)73723-3

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Article Doi

STEREOSELECTIVE APPROACH TO TRISUBSTITUTED TETRAHYDROFURANS

DOI: 10.1016/S0040-4039(00)73723-3

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(00)73723-3

Full text of DOI:10.1016/S0040-4039(00)73723-3

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