Abstract
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 bromohydrin.
Original language | English |
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Pages (from-to) | 3345-3357 |
Number of pages | 13 |
Journal | Synthetic Communications |
Volume | 28 |
Issue number | 18 |
DOIs | |
Publication status | Published - 1998 |
ASJC Scopus subject areas
- Organic Chemistry