1428883-53-7

Upstream product

• 1029033-63-3 but-3-ene-1-amine hydrobromide 
• 6630-33-7 ortho-bromobenzaldehyde 
• 2524-49-4 3-butene-1-amine 

Downstream Products

• 1029033-64-4 N-(2-bromobenzyl)but-3-ene-1-amine 
• 1352166-34-7 benzyl 2-(2-bromophenyl)-2,3,6,7-tetrahydro-1H-azepine-1-carboxylate 
• 1352166-33-6 benzyl (1-(2-bromophenyl)but-3-en-1-yl)(but-3-en-1-yl)carbamate 
• 1428883-57-1 N-(1-(2-bromophenyl)-3-phenylprop-2-yn-1-yl)-N-(but-3-en-1-yl)benzamide 
• 1428883-78-6 N-(1-(2-bromophenyl)-3-(4-methoxyphenyl)prop-2-yn-1-yl)-N-(but-3-en-1-yl)benzamide 
• 1428883-77-5 N-(1-(2-bromophenyl)-3-(4-fluorophenyl)prop-2-yn-1-yl)-N-(but-3-en-1-yl)benzamide 

Relevant academic research and scientific papers

Facile syntheses of substituted, conformationally-constrained benzoxazocines and benzazocines via sequential multicomponent assembly and cyclization

A multicomponent assembly process (MCAP) was utilized to prepare versatile intermediates that are suitably functionalized for subsequent cyclizations via Ullmann and Heck reactions to efficiently construct substituted 2,6-methanobenzo[b][1,5]oxazocines an

Ring-closing metathesis and ring-closing metathesis-isomerisation approach to 1-phosphonylated 2-benzazocines

An RCM strategy has been developed for the synthesis of phosphonylated benzazocines and their corresponding isomerised analogues. The aminophosphonate precursors were obtained by a one-pot three-component condensation in moderate yield.