144019-93-2

Upstream product

• 4746-93-4 1,4-dioxaspiro[4.5]decane-6-carboxylic acid 
• 13747-72-3 ethyl 1,4-dioxa-spiro[4,5]decane-6-carboxylate 
• 144019-65-8 3-(benzyloxy)-7,8,9,10-tetrahydrophenanthridine 
• 144019-57-8 N-(3-hydroxyphenyl)-1,4-dioxaspiro<4.5>decane-6-carboxamide 
• 144019-56-7 3-<1,4-dioxaspiro<4.5>decane-6-carbonyl>-1,3-thiazolidine-2-thione 
• 144019-66-9 3-(benzyloxy)-7,8,9,10-tetrahydrophenanthridine N-oxide 
• 144019-70-5 10-<(tert-butyldimethylsilyl)oxy>-3-hydroxy-7,8,9,10-tetrahydrophenanthridine 
• 144019-68-1 3-(benzyloxy)-10-hydroxy-7,8,9,10-tetrahydrophenanthridine 
• 144019-67-0 10-acetoxy-3-(benzyloxy)-7,8,9,10-tetrahydrophenanthridine 
• 144019-58-9 N-<3-(benzyloxy)phenyl>-1,4-dioxaspiro<4.5>decane-6-carboxamide 
• 144019-69-2 3-Benzyloxy-10-[(tert-butyldimethylsilyl)oxy]-7,8,9,10-tetrahydro-phenanthridine 
• 1655-07-8 ethyl 2-oxocyclohexane carboxylate 
• 3958-60-9 2-nitrophenylmethyl bromide 
• 144019-91-0 N-<(phenyloxy)carbonyl>-10-<(tert-butyldimethylsilyl)oxy>-3-<(2-nitrobenzyl)oxy>-6-<6-(trimethylsilyl)-3(Z)-hexene-1,5-diynyl>-5,6,7,8,9,10-hexahydrophenanthridine 

Downstream Products

• 144019-96-5 C₃₅H₂₆N₂O₈ 
• 144019-95-4 N-<(phenyloxy)carbonyl>-6a,10a-epoxy-6-<3(Z)-hexene-1,5-diynyl>-3-<(2-nitrobenzyl)oxy>-10-oxo-5,6,6a,7,8,9,10,10a-octahydrophenanthridine 
• 144019-97-6 C₃₀H₂₃NO₇ 
• 144019-98-7 C₃₀H₂₉NO₇ 
• 144071-89-6 C₂₈H₂₁NO₆ 
• 135106-78-4 C₂₈H₂₇NO₅S 
• 135144-02-4 C₂₈H₂₇NO₆ 
• 144041-66-7 C₃₃H₂₄N₂O₇ 
• 135106-86-4 C₂₈H₂₁NO₇ 
• 135106-79-5 C₂₇H₂₁NO₅ 
• 135144-04-6 C₂₆H₁₉NO₆ 
• 135106-77-3 C₂₆H₁₉NO₅ 
• 144019-94-3 N-<(phenyloxy)carbonyl>-6-<3(Z)-hexene-1,5-diynyl>-3-<(2-nitrobenzyl)oxy>-10-oxo-5,6,7,8,9,10-hexahydrophenanthridine 

Relevant academic research and scientific papers

Molecular design and chemical synthesis of potent enediynes. 2. Dynemicin model systems equipped with C-3 triggering devices and evidence for quinone methide formation in the mechanism of action of dynemicin A

Continuing the theme of the preceding article, this paper describes the synthesis and chemical properties of designed enediynes related to dynemicin A. These model systems are equipped with triggering devices at C-3 of the aromatic nucleus. The design of