New stereoselective beta-C-glycosidation by uncatalyzed 1,4-addition of organolithium reagents to a glycal-derived vinyl oxirane

Org Lett. 2003 Jun 12;5(12):2173-6. doi: 10.1021/ol034662f.

Abstract

[reaction: see text] Epoxide 4 is generated in situ from d-glucal-derived hydroxy mesylate 3. Reaction of epoxide 4 with a series of alkyl- and aryllithium reagents affords 2,3-unsaturated beta-C-glycosides with excellent 1,4-regioselectivity and complete stereoselectivity for the beta-glycoside. Other organometallic reagents demonstrate more complex behavior in their reactions with epoxide 4.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ethylene Oxide / chemistry*
  • Glucosides / chemical synthesis*
  • Glycosylation
  • Lithium / chemistry*
  • Organometallic Compounds / chemistry*
  • Stereoisomerism

Substances

  • Glucosides
  • Organometallic Compounds
  • Lithium
  • Ethylene Oxide