Bile alcohol glucuronides: regioselective O-glucuronidation of 5β-cholestane-3α,7α,12α,25-tetrol and 24-nor-5β-cholestane-3α,7α,12α,25-tetrol

✍ Scribed by Bishambar Dayal; Gerald Salen; Janak Padia; Sarah Shefer; George S. Tint; Gino Sasso; Tomas H. Williams

• Publisher: Elsevier Science
• Year: 1993
• Tongue: English
• Weight: 746 KB
• Volume: 240
• Category: Article
• ISSN: 0008-6215
• DOI: 10.1016/0008-6215(93)84178-9

✦ Synopsis

ABSTRAm

A facile and regiocontrolled procedure for the preparation of S~-cholestane-3a,7c,l2~,25-tetrol-3-O-fi-o-glucuronide and its corresponding C-26 analogue is described. The method involves direct coupling of bile alcohols, namely, 5/3-cholestane-3rY,7~,12a,25-tetrol and 24-nor-Sp-cholestane-3a,7u,12a,25tetrol

to methyl (tetra-0-acetyl$-o-glucopyranuronate) in the presence of a Lewis acid, tin(W) chloride, in dichloromethane.

The resulting anomeric pairs of 1,2-rrarul-and 1,2-cis-glucuronides of tetrols were resolved by analytical and preparative thin-layer chromatography, and their identities were established by high-resolution 'H NMR spectroscopy and by chemical-ionization and fast-atombombardment mass spectrometry. The method described has a practical advantage over the traditional two-step synthesis involving bromides as it is more efficient and uses inexpensive and less toxic materials.

It is suggested that these compounds will be useful for studying permeability of the blood-brain barrier in cerebrotendinous xanthomatosis (CTX).