888030-07-7

Upstream product

• 888030-06-6 2-(2-iodo-5-methoxyphenyl)acetamide 
• 1694-92-4 2-Nitrobenzenesulfonyl chloride 
• 112399-38-9 (2-Iodo-5-methoxy-phenyl)-acetyl chloride 
• 73029-52-4 2-(2-iodo-5-methoxyphenyl)acetic acid 

Downstream Products

• 888029-96-7 N-Boc-N-nosyl-2-(2-iodo-5-methoxyphenyl)ethanamine 
• 888030-01-1 N-Boc-N-nosyl-2-(4-(2-(2-aminoethyl)-4-methoxyphenyl)-1-methoxycyclohex-3-enyl)ethanol 
• 888030-10-2 N-nosyl-2-(4-(2-(2-aminoethyl)-4-methoxyphenyl)-1-methoxycyclohex-3-enyl)ethanol 
• 888030-11-3 5,13-dimethoxy-10-(2-nitro-benzenesulfonyl)-10-aza-tricyclo[11.2.2.0^2,7]heptadeca-1⁽¹⁶⁾,2⁽⁷⁾,3,5-tetraen-15-ol 
• 888030-03-3 N-nosyl-4-aza-4'-methoxybenzo[2',1'-g]bicyclo[7.2.2]tridec-9⁽¹³⁾-en-10-one 
• 888030-02-2 N-nosyl-4-aza-4'-methoxybenzo[2',1'-g]bicyclo[7.2.2]tridec-9⁽¹⁰⁾-ene 
• 888030-04-4 N-nosyl-1²,2⁴-dimethoxy-5-aza-1(1,4),2(1,2)-dibenzenacycloheptaphane 

Relevant academic research and scientific papers

Synthesis of the 3-aza-[7]-paracyclophane core of haouamine A and B

The synthesis of the highly strained 3-aza-[7]-paracyclophane core of haouamines A and B is based on a macrocyclization-aromatization protocol, allowing for a stepwise increase in ring strain and establishing the oxygenation pattern of the natural product