302964-50-7

Upstream product

• 302964-56-3 (S)-4-benzyloxy-3-(7-bromo-2-hydroxy-1,2-dihydrobenzo[b]furan-3-yl)-N-(benzyloxycarbonyl)tyrosine tert-butyl ester 
• 16881-33-7 (S)-tert-butyl 2-(((benzyloxy)carbonyl)amino)-3-(4-hydroxyphenyl)propanoate hydrate 
• 70-78-0 3-Iodo-L-tyrosine 
• 79677-62-6 (S)-2-(((benzyloxy)carbonyl)amino)-3-(4-hydroxy-3-iodophenyl)propanoic acid 
• 870456-12-5 (S)-N-benzyloxycarbonyl-3-iodotyrosine tert-butyl ester 
• 302964-51-8 (S)-4-benzyloxy-3-iodo-N-(benzyloxycarbonyl)tyrosine tert-butyl ester 
• 302964-52-9 (S)-4-benzyloxy-3-(3-hydroxypropenyl)-N-(benzyloxycarbonyl)tyrosine tert-butyl ester 
• 302964-53-0 (S)-4-benzyloxy-3-(3-bromopropenyl)-N-(benzyloxycarbonyl)tyrosine tert-butyl ester 
• 302964-54-1 (S)-4-benzyloxy-3-(3-(2-bromophenoxy)propenyl)-N-(benzyloxycarbonyl)tyrosine tert-butyl ester 
• 302964-55-2 (S)-4-benzyloxy-3-(1-(3-bromo-2-hydroxyphenyl)prop-2-enyl)-N-(benzyloxycarbonyl)tyrosine tert-butyl ester 
• 501-53-1 benzyl chloroformate 

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 a tyrosine-derived benzofuranone

The benzofuranone 2, a potential intermediate for the synthesis of the marine natural product diazonamide A 1, has been synthesised in eight steps from the N-protected tyrosine ester 3. (C) 2000 Elsevier Science Ltd.