1403934-35-9

Upstream product

• 110-52-1 1,4-dibromo-butane 
• 32975-62-5 (S)-(+)-5-methyl-4-phenyl-1,5-diazacyclooctan-2-one 

Downstream Products

• 49620-05-5 (4′S,4''R,2'''R)-1-[2'-oxo-4′-phenyl-N(5')-methyl-1',5'-diazocan-N(1′)-yl]-4-[2''-oxo-4''-(2'''-hydroxyheptyl)-N(5'')-methyl-1'',5''-diazocan-N(1'')-yl]butane 
• 1404225-53-1 (S,S,S)-1-[2'-oxo-4′-phenyl-N(5')-methyl-1',5'-diazocan-N(1′)-yl]-4-[2''-oxo-4''-(2'''-hydroxyheptyl)-N(5'')-methyl-1'',5''-diazocan-N(1'')-yl]butane 
• 1404225-51-9 (4′S,4''R,2'''S)-1-[2'-oxo-4′-phenyl-N(5')-methyl-1',5'-diazocan-N(1′)-yl]-4-[2''-oxo-4''-(2'''-hydroxyheptyl)-N(5'')-methyl-1'',5''-diazocan-N(1'')-yl]butane 
• 1404225-52-0 (4′S,4''S,2'''R)-1-[2'-oxo-4′-phenyl-N(5')-methyl-1',5'-diazocan-N(1′)-yl]-4-[2''-oxo-4''-(2'''-hydroxyheptyl)-N(5'')-methyl-1'',5''-diazocan-N(1'')-yl]butane 

Relevant academic research and scientific papers

Absolute configuration assignment by asymmetric syntheses of the homalium alkaloids (?)-(R, R, R)-hoprominol and (?)-(4′ S,4″ R,2? R)-Hopromalinol

The conjugate addition of lithium (R)-N-(3-chloropropyl)-N-(α- methylbenzyl)amide to α,β-unsaturated esters was used as the key step in the syntheses of all possible diastereoisomers of the homalium alkaloids hoprominol and hopromalinol. Comparison of the