124575-15-1

Upstream product

• 18964-33-5 2-(toluene-4-sulfonyl)-2-aza-bicyclo[2.2.1]heptan-3-one 
• 98-59-9 p-toluenesulfonyl chloride 
• 49805-30-3 2-azabicyclo[2.2.1.]hept-5-en-3-one 
• 109000-07-9 2-(p-tolylsulfonyl)-2-azabicyclo<2.2.1>hept-5-en-3-one 

Relevant academic research and scientific papers

Synthesis and reactivity of azapalladacyclobutanes

N-Sulfonyl aziridines undergo oxidative addition to palladium(O) complexes generated in situ from mixtures of Pd2(dba)3 and 1,10-phenanthroline. The resulting azapalladacyclobutane complexes undergo intramolecular carbopalladation in

STEREOSPECIFIC SYNTHESIS OF CARBOCYCLIC NUCLEOSIDES FROM 2-AZABICYCLO-HEPTAN-3-ONES VIA SODIUM BOROHYDRIDE MEDIATED CARBON-NITROGEN BOND CLEAVAGE

New synthons for carbocyclic nucleosides have been synthesized from 2-azabicyclohept-5-en-3-one readily available from cyclopentadiene, through introduction of an electron-withdrawing substituent at the 2-position followed by reduction with sodium