Modular access to N-substituted cis-3,5-diaminopiperidines.

J Org Chem

Laboratoire de Chimie et de Biochimie Pharmacologiques et Toxicologiques, Faculté des Sciences Fondamentales et Biomédicales, UMR8601, CNRS-Paris Descartes University, 45 rue des Saints Pères, 75006 Paris, France.

Published: December 2013

A sequence of oxidative cleavage/reductive amination/hydrogenolysis enables the preparation of N-substituted cis-3,5-diaminopiperidines from a readily available bicyclic hydrazine. This new synthetic route provides a simple and general access to RNA-friendly fragments with a good chemical diversity.

Download full-text PDF

Source
http://dx.doi.org/10.1021/jo401994yDOI Listing

Publication Analysis

Top Keywords

n-substituted cis-35-diaminopiperidines
8
modular access
4
access n-substituted
4
cis-35-diaminopiperidines sequence
4
sequence oxidative
4
oxidative cleavage/reductive
4
cleavage/reductive amination/hydrogenolysis
4
amination/hydrogenolysis enables
4
enables preparation
4
preparation n-substituted
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!