577705-94-3

Upstream product

• 577705-93-2 1-benzyloxy-3-[(tert-butyloxycarbonyl)amino]isoquinoline 
• 24424-99-5 di-tert-butyl dicarbonate 
• 13130-79-5 3-amino-1-bromoisoquinoline 
• 20194-18-7 sodium phenyl-methanolate 
• 577705-92-1 3-amino-1-benzyloxyisoquinoline 
• 100-51-6 benzyl alcohol 

Downstream Products

• 577705-95-4 3-[N-(tert-butyloxycarbonyl)-N-(3-chloroprop-2-en-1-yl)amino]-1-benzyloxy-4-iodoisoquinoline 
• 577705-96-5 5-benzyloxy-3-N-(tert-butyloxycarbonyl)-1-(chloromethyl)-1,2-dihydropyrrolo[2,3-c]isoquinoline 
• 577705-97-6 (S)-5-benzyloxy-3-N-(tert-butyloxycarbonyl)-1-(chloromethyl)-1,2-dihydropyrrolo[2,3-c]isoquinoline 
• 577705-98-7 (R)-5-benzyloxy-3-N-(tert-butyloxycarbonyl)-1-(chloromethyl)-1,2-dihydropyrrolo[2,3-c]isoquinoline 

Relevant academic research and scientific papers

Synthesis and Evaluation of Duocarmycin and CC-1065 Analogues Incorporating the 1,2,9,9a-Tetrahydrocyclopropa[c]benz[e]-3-azaindol-4-one (CBA) Alkylation Subunit

An efficient eight-step synthesis (53% overall) and the evaluation of 1,2,9,9a-tetrahydrocyclopropa-[c]benz[e]-3-azaindol-4-one (CBA) and its derivatives containing an aza variant of the CC-1065/ duocarmycin alkylation subunit are detailed. This unique de

Synthesis and X-ray analysis of an unprecedented and stable 2-aza-4,4-spirocyclopropacyclohexadienone

(Matrix presented) An efficient eight-step synthesis (54% overall) and the subsequent X-ray characterization of 1,2,9,9a-tetrahydrocyclopropa[c]benz[e]-3-azaindol-4-one (CBA) containing an aza variant of the CC-1065/duocarmycin alkylation subunit are deta