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New stereoselective reaction of methylglyoxal with 2-aminopyridine and adenine derivatives: Formation of imino acid-nucleic base derivatives in water under mild conditions
Christel Routaboul,Lionel Dumas,Isabelle Gautier-Luneau,Jacques Vergne,Marie-Christine Maurel,Jean-Luc Décout
Chemical Communications Pub Date : 04/23/2002 00:00:00 , DOI:10.1039/B201901A
Abstract

A remarkable stereoselective reaction of methylglyoxal with 2-aminopyridine, the nucleic base adenine and adenine nucleosides leads in good yield to heterocycles of a new family in water under mild conditions and should be of interest in the understanding of the biological effects of methylglyoxal which is toxic, mutagenic and involved in diabetic complications.

Graphical abstract: New stereoselective reaction of methylglyoxal with 2-aminopyridine and adenine derivatives: Formation of imino acid-nucleic base derivatives in water under mild conditions
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