303068-11-3

Upstream product

• 98600-34-1 4-bromo-1H-indole-3-carbaldehyde 
• 108061-74-1 2-(4-bromo-1H-indol-3-yl)ethan-1-amine 
• 52488-36-5 4-bromo-1H-indole 
• 303068-04-4 4-bromo-3-[(E)-2-nitro-1-ethenyl]-1H-indole 
• 303068-09-9 ethyl 4-{3-[1-tert-butoxycarbonyl-3-(2-tert-butoxycarbonylaminoethyl)indol-4-yl]-2-methoxyphenyl}-3-oxobutanoate 
• 303068-07-7 4-(3-allyl-2-methoxyphenyl)-N,N'-di-tert-butoxycarbonyltryptamine 
• 303068-08-8 3-[1-tert-butoxycarbonyl-3-(2-tert-butoxycarbonylaminoethyl)indol-4-yl]-2-methoxyphenylacetaldehyde 
• 303068-05-5 tert-butyl 4-bromo-3-(2-((tert-butoxycarbonyl)amino)ethyl)-1H-indole-1-carboxylate 
• 303068-06-6 3-allyl-2-methoxybenzeneboronic acid 
• 88275-72-3 3-Brom-2-methoxy-1-(2-propenyl)benzol 
• 60333-75-7 O-allyl-2-bromophenol 
• 17269-81-7 2-bromo-6-(2-propenyl)phenol 
• 870456-21-6 3-(2-tert-butoxycarbonylamino-ethyl)-4-[3-(2,3-dihydroxy-propyl)-2-methoxy-phenyl]-indole-1-carboxylic acid tert-butyl ester 
• 303068-04-4 4-bromo-3-(2-nitroethenyl)-indole 

Relevant academic research and scientific papers

The diazo route to diazonamide A: Studies on the tyrosine-derived fragment

Various approaches to the tyrosine-derived fragment of the marine secondary metabolite diazonamide A are described. Initial efforts were focused on the originally proposed structure of the natural product, and a feasibility study established that a model

Studies towards the synthesis of diazonamide A. Synthesis of the 4-(oxazol-5-ylmethyl) aryltryptamine fragment

The oxazole substituted 4-aryltryptamine 5, a potential intermediate for the synthesis of the marine natural product diazonamide A 1, has been synthesised. (C) 2000 Elsevier Science Ltd.