1053643-34-7

Upstream product

• 70337-25-6 4,5-O-isopropylidene-D-arabinose diethyldithioacetal 
• 824-94-2 p-methoxybenzyl chloride 
• 153098-16-9 2,3-Bis(p-methoxybenzyl)-1,1-bis(ethylthio)-4,5-isopropylidene-D-arabinose 

Downstream Products

• 153154-88-2 N-(2-Oxopropyl)-2-(N-benzoylamino)-4(R),5(R)-bis<(p-methoxybenzyl)oxy>-5--2(Z)-pentenamide 
• 153098-22-7 (2'S)-3--2(R),3(R)-bis<(p-methoxybenzyl)oxy>-1-O-(tert-butyldiphenylsilyl)propanol 
• 1053697-36-1 Methanesulfonic acid (2R,3R,4R)-5-(tert-butyl-diphenyl-silanyloxy)-2-hydroxy-3,4-bis-(4-methoxy-benzyloxy)-pentyl ester 
• 153154-91-7 N-[(Z)-(3S,4R)-4-(S)-Aziridin-2-yl-2-bromo-3,4-bis-(4-methoxy-benzyloxy)-1-(2-oxo-propylcarbamoyl)-but-1-enyl]-benzamide 
• 153098-23-8 (2'-S)-3--2(R),3(R)-bis<(p-methoxybenzyl)oxy>-1-propanol 
• 153098-21-6 (2'S)-3-(2'-Aziridinyl)-2(R),3(R)-bis<(p-methoxybenzyl)oxy>-1-O-(tert-butyldiphenylsilyl)propanol 
• 139427-62-6 Ethyl 2-(N-Benzoylamino)-2(E)-<3(R),4(R)-bis<(p-methoxybenzyl)oxy>-5(S)-1-azabicyclo<3.1.0>hex-2-ylidene>acetate 
• 139427-61-5 Ethyl (E)-2-(N-benzoylamino)-3-bromo-4(S),5(R)-bis<(p-methoxybenzyl)oxy>-5--2-pentenoate 
• 139560-99-9 Ethyl (Z)-2-(N-benzoylamino)-3-bromo-4(S),5(R)-bis<(p-methoxybenzyl)oxy>-5--2-pentenoate 
• 139559-29-8 Ethyl (Z)-2-(N-benzoylamino)-4(R),5(R)-bis<(p-methoxybenzyl)oxy>-5--2-pentenoate 
• 139559-28-7 Ethyl (E)-2-(N-Benzoylamino)-4(R),5(R)-bis<(p-methoxybenzyl)oxy>-5--2-pentenoate 
• 137845-83-1 (2'S)-3--2(R),3(R)-bis<(p-methoxybenzyl)oxy>-1-propanal 
• 139427-63-7 (E)-(4S,5R)-5-(S)-Aziridin-2-yl-2-benzoylamino-3-bromo-4,5-bis-(4-methoxy-benzyloxy)-pent-2-enoic acid ethyl ester 

Relevant academic research and scientific papers

Dehydroamino acid derivatives from D-arabinose and L-serine: Synthesis of models for the azinomycin antitumor antibiotics

Synthesis of aldehydes 17 from D-arabinose and 31 from L-serine provided key precursors for the generation of highly functionalized dehydroamino acid derivatives upon condensation with glycyl phosphonates. Subsequent bromination and intramolecular additio