257907-98-5

Upstream product

• 126275-19-2 (R)-N-allyl (1-phenylethyl)amine 
• 257907-89-4 tert-Butyl (3S,αR)-(E)-3-[N-(benzyloxycarbonyl)-N-(α-methylbenzyl)amino]hex-4-enoate 
• 257907-91-8 (4S,5R,1'S,αR)-4-[(tert-Butoxycarbonyl)methyl]-5-(1'-iodoethyl)-3-(α-methylbenzyl)oxazolidin-2-one 
• 257907-87-2 tert-Butyl (3S,αR)-(E)-3-[N-(α-methylbenzyl)amino]hex-4-enoate 
• 3886-69-9 (R)-1-phenyl-ethyl-amine 
• 257907-97-4 (4S,5R,1'S,αR)-(E)-4-Carboxymethyl-5-(1'-iodoethyl)-3-(α-methylbenzyl)oxazolidin-2-one 
• 257907-90-7 tert-Butyl (3S,αR)-(E)-3-[N-(tert-butoxycarbonyl)-N-(α-methylbenzyl)amino]hex-4-enoate 

Relevant academic research and scientific papers

Syntheses of derivatives of L-daunosamine and its C-3 epimer employing as the key step the asymmetric conjugate addition of a homochiral lithium amide to tert-butyl (E,E)-hexa-2,4-dienoate

The highly diastereoselective asymmetric conjugate addition of lithium (R)-N-benzyl-α-methylbenzylamide to methyl or tert-butyl (E,E)-hexa-2,4-dienoate, followed by osmium tetroxide-catalysed dihydroxylation of the resulting adducts, provides a concise ro