1569438-35-2

Upstream product

• 1360895-23-3 (E)-2,3-dibromo-4-methylpent-2-enoic acid 
• 4903-09-7 3-chloro-4-methoxy-benzaldehyde 
• 1569438-65-8 2-chloro-4-(2,2-dibromovinyl)-1-methoxybenzene 
• 32363-92-1 1,1-dibromo-3-methyl-1-butene 
• 38491-47-3 ethyl 4-methylpent-2-ynoate 
• 65199-69-1 4-methyl-2-pentynoic acid 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 1569438-14-7 (Z)-3-benzyl-5-(3-chloro-4-methoxybenzylidene)-4-isopropylfuran-2(5H)-one 
• 1569438-20-5 (Z)-5-(3-chloro-4-methoxybenzylidene)-4-isopropyl-3-(3-methoxybenzyl)furan-2(5H)-one 
• 1569438-22-7 (5Z)-5-[(3-chloro-4-methoxyphenyl)methylidene]-3-[(4-fluorophenyl)methyl]-4-(propan-2-yl)-2,5-dihydrofuran-2-one 

Relevant academic research and scientific papers

Copper-catalyzed domino route to natural nostoclides and analogues: A total synthesis of nostoclides i and II

An original and convenient domino route to natural nostoclides I and II has been developed using a two-step sequence consisting of a copper-cat-alyzed tandem reaction associated with Suzuki cross-coupling. The methodology employed for this total synthesis appeared to be an interesting and suffi-ciently flexible tool to allow the synthesis of numer-ous analogues of these nostoclides.