873843-75-5

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 43192-31-0 2-bromo-4-methoxybenzaldehyde 
• 873843-73-3 (Z)-3-(2-bromo-4-methoxyphenyl)-2-tert-butoxycarbonylaminoacrylic acid methyl ester 

Downstream Products

• 925452-26-2 C₁₁H₁₄BrNO₃S 
• 873843-72-2 (R)-4-(2-bromo-4-methoxybenzyl)-3-methyl-1,2,3-oxathiazolidine 2,2-dioxide 
• 1025995-08-7 (R)-4-(2-bromo-4-methoxybenzyl)-3-methyloxazolidin-2-one 
• 873843-76-6 (R)-3-(2-bromo-4-methoxyphenyl)-2-(methylamino)propan-1-ol 
• 1026299-19-3 C₁₁H₁₂BrNO₃ 

Relevant academic research and scientific papers

Cyclic sulfamidates as lactam precursors. An efficient asymmetric synthesis of (-)-aphanorphine

A short and efficient enantioselective synthesis of (-)-aphanorphine is described based on the use of a cyclic sulfamidate to provide a suitably functionalised lactam that allows for construction of the tricyclic 3-benzazepine scaffold. The Royal Society