136964-88-0

Upstream product

• 5927-18-4 trimethyl phosphonoacetate 
• 120205-96-1 (S)-2-(dibenzylamino)propanal 
• 87281-16-1 2-dibenzylamino-propionic acid methyl ester 
• 88738-78-7 bis-(2,2,2-trifluoroethyl)(methoxycarbonylmethyl)phosphonate 

Downstream Products

• 138041-15-3 Dibenzyl-((E)-(1S,4R)-1-methyl-4-trimethylsilanyloxy-oct-2-enyl)-amine 
• 138041-21-1 Dibenzyl-((E)-(1S,4S)-1-methyl-4-trimethylsilanyloxy-oct-2-enyl)-amine 
• 138041-20-0 Dibenzyl-((E)-(1S,4S)-1-methyl-4-trimethylsilanyloxy-pent-2-enyl)-amine 
• 138041-14-2 Dibenzyl-((E)-(1S,4R)-1-methyl-4-trimethylsilanyloxy-pent-2-enyl)-amine 
• 138041-56-2 (E)-(S)-4-Dibenzylamino-pent-2-enal 
• 155626-84-9 (4S,2E)-4-(N,N-dibenzylamino)pent-2-en-1-ol 
• 138041-45-9 (Z)-(3S,6S)-6-Dibenzylamino-3-hydroxy-hept-4-enoic acid phenyl ester 
• 138041-30-2 (Z)-(3R,6S)-6-Dibenzylamino-3-hydroxy-hept-4-enoic acid phenyl ester 
• 138041-44-8 (Z)-(3S,6S)-6-Dibenzylamino-3-hydroxy-hept-4-enoic acid methyl ester 
• 138041-29-9 (Z)-(3R,6S)-6-Dibenzylamino-3-hydroxy-hept-4-enoic acid methyl ester 
• 138041-31-3 (Z)-(3S,6S)-6-Dibenzylamino-3-hydroxy-2,2-dimethyl-hept-4-enoic acid methyl ester 
• 138041-46-0 (Z)-(3R,6S)-6-Dibenzylamino-3-hydroxy-2,2-dimethyl-hept-4-enoic acid methyl ester 
• 138041-43-7 (Z)-(2S,5S)-2-Dibenzylamino-non-3-en-5-ol 
• 138041-28-8 (Z)-(2S,5R)-2-Dibenzylamino-non-3-en-5-ol 

Relevant academic research and scientific papers

One-pot synthesis of enantiomerically pure N-protected allylic amines from N-protected α-amino esters

An improved protocol for the synthesis of enantiomerically pure allylic amines is reported. N-Protected α-amino esters derived from natural amino acids were submitted to a one-pot tandem reduction-olefination process. The sequential reduction with DIBAL-H

Novel 1,4-Asymmetric Induction in Nucleophilic 1,2-Additions to Chiral γ-Amino Enals

γ-Dibenzylamino enals 3a with the E-configuration derived from amino acids 1 react diastereoselectively with cuprates in an unexpected 1,2-manner, while the analogues 3b with the Z-configuration undergo diastereoselective additions with organolithium reagents.