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. Author manuscript; available in PMC: 2008 Dec 10.
Published in final edited form as: Carbohydr Res. 2007 Aug 19;342(17):2575–2592. doi: 10.1016/j.carres.2007.08.003

Scheme 1.

Scheme 1

Proposed early reactions of R5P (1) with amines stemming from the acyclic form in equilibrium with the furanose. A traditional series of Maillard reactions (path A) leads through an Amadori product (2) to an α-dicarbonyl product (3), while an isomerization series (path B) leading to ribulose 5-phosphate (4) may be encouraged by a general base catalysis (i.e., removal of the C-2 hydrogen) of the amine.