477203-69-3

Upstream product

• 958633-78-8 C₁₉H₁₈N₂O₅ 
• 958633-72-2 C₁₆H₁₆N₂O₅ 
• 958633-73-3 C₁₆H₁₈N₂O₃ 
• 958633-74-4 6-methoxy-3-(4-methoxy-2-methylphenyl)quinazolin-4(3H)-one 
• 102-50-1 2-methyl-4-methoxyaniline 
• 2327-45-9 methyl 2-nitro-5-(methoxy)benzoate 
• 2475-80-1 methyl 2-amino-5-methoxybenzoate 
• 1882-69-5 5-methoxy-2-nitro-benzoic acid 
• 55414-72-7 (2-amino-5-methoxyphenyl)methanol 
• 1313233-42-9 methyl 2-formylamino-5-methoxybenzoate 
• 64-18-6 formic acid 
• 77287-34-4 formamide 

Downstream Products

• 958633-80-2 C₁₇H₂₀N₂O₃ 
• 958633-81-3 C₁₇H₁₈N₂O₄ 

Relevant academic research and scientific papers

Concise Synthesis of Dictyoquinazol A via a Dimerisation-Cyclocondensation Sequence

A two-step total synthesis of the neuroprotective alkaloid, dictyoquinazol A, has been achieved. The brevity of this synthesis was enabled by exploiting the hidden symmetry of the target molecule. Several structural analogues were also prepared using a similar strategy. These results provide a platform for future structure-activity relationship studies in the quest for a novel treatment for stroke.

Synthesis and neuroprotective activity of dictyoquinazol A and analogues

A flexible and efficient synthesis of the neuroprotective alkaloid, dictyoquinazol A, is reported. Several structural analogues of the target molecule were produced, and the neuroprotective activity of this series of compounds was investigated using three

Total synthesis of neuroprotective dictyoquinazol A, B, and C

A new protective compound, dictyoquinazol A, was synthesized starting from 5-methoxy-2-nitrobenzoic acid in six-steps in 36% overall yield. Two derivatives B and C, isolated from the mushroom Dictyophora indusiata, were also synthesized from Dictyoquinazo