220585-29-5

Upstream product

• 76412-28-7 4-bromo-4'-methoxy-α,α'-diethyl-trans-stilbene 
• 220585-28-4 {4-[(E)-1-Ethyl-2-(4-methoxy-phenyl)-but-1-enyl]-phenyl}-methanol 
• 3433-80-5 1-Bromo-2-bromomethyl-benzene 

Downstream Products

• 220585-33-1 {2-[4-(2-{4-[(E)-1-Ethyl-2-(4-methoxy-phenyl)-but-1-enyl]-benzyloxymethyl}-phenyl)-buta-1,3-diynyl]-phenyl}-methanol 
• 220585-25-1 1-{2-[4-(2-{4-[(E)-1-Ethyl-2-(4-methoxy-phenyl)-but-1-enyl]-benzyloxymethyl}-phenyl)-buta-1,3-diynyl]-phenyl}-5-trimethylsilanyl-penta-2,4-diyn-1-ol 

Relevant academic research and scientific papers

An unprecedented arylcarbene formation in thermal reaction of non- conjugated aromatic enetetraynes and DNA strand cleavage

The thermal cyclization of non-conjugated aromatic enetetrayne (4) led to the final products (2 and 10) affording 5H-12- hydroxybenzol[d]fluorenol[3,2-b]pyran radical (C) and arylcarbene (D) intermediates. DNA strand cleavage was observed.