cis-2,5-Disubstituted Tetrahydrofurans from Pyranosides: A Novel Example of Remote Stereocontrol by the Aglycone

DOI: 10.1016/0040-4039(94)02342-9

Source and publish data:

Tetrahedron Letters p. 649 - 652 (1995)

Update date:2022-07-30

Topics: Aglycone Cis-2,5-Disubstituted Tetrahydrofurans Pyranosides Remote Stereocontrol

Authors:

Zhang, Huiping

Wilson, Phyllis

Shan, Weifang

Ruan, Zheming

Mootoo, David R.

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Article abstract of DOI:10.1016/0040-4039(94)02342-9

A stereoselective methodology, based on neighboring group participation by the acetal ring oxygen, is described for the preparation of highly functionalizable cis-2,3-disubstituted tetrahydrofurans from C6 alkenyl branched pyranosides.

Full text of DOI:10.1016/0040-4039(94)02342-9

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