Skip to Content
Merck
  • Imino-C-nucleoside synthesis: heteroaryl lithium carbanion additions to a carbohydrate cyclic imine and nitrone.

Imino-C-nucleoside synthesis: heteroaryl lithium carbanion additions to a carbohydrate cyclic imine and nitrone.

The Journal of organic chemistry (2004-04-03)
Gary B Evans, Richard H Furneaux, Herwig Hausler, Janus S Larsen, Peter C Tyler
ABSTRACT

Promotion by Lewis acid of the addition of some aryllithiums to a carbohydrate-based imine, which has allowed a more facile synthesis of some imino-C-nucleoside analogues, is described. Use of the corresponding nitrone does not assist in some cases, but lithiated acetonitrile adds to it efficiently to give a product from which further C-nucleoside analogues can be derived.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Tin(IV) chloride, 98%
Sigma-Aldrich
Tin(IV) chloride solution, 1.0 M in methylene chloride
Sigma-Aldrich
Tin(IV) chloride, 99.995% trace metals basis