1309952-39-3

Upstream product

• 49675-21-0 dibenzyl 2,3-diazabicyclo[2.2.1]hept-5-ene-2,3-dicarboxylate 

Downstream Products

• 1309952-40-6 3,5-bis-(2,6-dinitrophenylamino)cyclopentane-1,2-diol 
• 1309952-46-2 4-oxo-3,5-dioxa-4-thia-8,9-diazatricyclo[5.2.1.0(2,6)]decane-8,9-dicarboxylic acid dibenzyl ester 

Relevant academic research and scientific papers

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

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.

Stereoselective synthesis of fluorinated 1,3- cis -diaminocyclopentanes

Several fluorinated 1,3-diaminocyclopentanes, previously reported to be useful RNA structural probes, can be prepared in a diastereoselective manner from a single bicyclic hydrazine precursor, in 3 to 9 steps.