145661-34-3

Upstream product

• 145661-33-2 10-(tert-Butyl-dimethyl-silanyloxy)-7,8-dihydro-phenanthridine 
• 1885-14-9 phenyl chloroformate 
• 4301-14-8 acetylenemagnesium bromide 
• 145661-32-1 8,9-Dihydro-7H-phenanthridin-10-one 
• 141328-93-0 10-hydroxy-7,8,9,10-tetrahydrophenanthridine 

Downstream Products

• 145661-35-4 C₂₆H₂₅NO₄ 
• 145772-99-2 C₃₃H₃₅NO₄Si 
• 145661-36-5 C₃₃H₃₅NO₄Si 
• 145773-00-8 C₃₀H₂₇NO₄ 
• 145661-37-6 C₃₀H₂₇NO₄ 
• 145773-01-9 C₂₆H₁₉NO₄ 
• 130012-96-3 C₂₆H₁₉NO₄ 
• 145661-38-7 (S)-6-((Z)-Hex-3-ene-1,5-diynyl)-10-oxo-7,8,9,10-tetrahydro-6H-phenanthridine-5-carboxylic acid phenyl ester 
• 145661-38-7 (R)-6-((Z)-Hex-3-ene-1,5-diynyl)-10-oxo-7,8,9,10-tetrahydro-6H-phenanthridine-5-carboxylic acid phenyl ester 

Relevant academic research and scientific papers

Synthesis and Biological Actions of Optically Active Enediynes Related to Dynemicin A

Enantiomerically pure enediynes (+)-2 and (-)-2 were synthesized using a chiral resolution method and were shown to exhibit different cytotoxicities against a number of tumour cells.