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  • Stereoselective synthesis of sugar fused β-disubstituted γ-butyro-lactones: C-spiro-glycosides from 1,2-cyclopropanecarboxylated sugars.

Stereoselective synthesis of sugar fused β-disubstituted γ-butyro-lactones: C-spiro-glycosides from 1,2-cyclopropanecarboxylated sugars.

Chemical communications (Cambridge, England) (2011-12-03)
Perali Ramu Sridhar, Kalapati Seshadri, Gadi Madhusudhan Reddy
ABSTRACT

A stereoselective methodology was developed for the construction of C-spiro-glycosides in two steps involving bromonium ion activated solvolytic ring opening of sugar derived 1,2-cyclopropanecarboxylates followed by a one-pot dehydrohalogenation, intramolecular hetero-Michael addition (IHMA) and ester hydrolysis. The obtained spirocyclic lactols were further converted to enantiomerically pure spirolactones.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Cyclopropanecarboxylic acid, 95%