A facile route to steroidal 6-deoxy-α-L-allopyranosides

DOI: 10.1080/00397919808004442

Source and publish data:

Synthetic Communications p. 3345 - 3357 (1998)

Update date:2022-08-03

Topics:

Authors:

Van Heerden, Fanie R.

Dixon, John T.

Holzapfel, Cedric W.

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Article abstract of DOI:10.1080/00397919808004442

The synthesis of a steroidal 6-deoxy-α-L-allopyranoside from cholestanol and rhamnose is described. The crucial steps in the reaction sequence comprised the transformation of a pseudoglycal into the more steric hindered 2,3-cisdiol via an intermediate bro

Full text of DOI:10.1080/00397919808004442

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