188409-89-4

Upstream product

• 188410-04-0 (E)-(S)-4-Benzyloxy-5-tert-butoxycarbonylamino-pent-2-enoic acid methyl ester 
• 24424-99-5 di-tert-butyl dicarbonate 
• 100-39-0 benzyl bromide 
• 143396-63-8 (R)-3-Amino-2-benzyloxy-propan-1-ol 
• 188409-88-3 N-[2R-3-hydroxy-2-(phenylmethoxy)propyl](tert-butoxy)carboxamide 
• 188410-03-9 ((R)-2-Benzyloxy-3-oxo-propyl)-carbamic acid tert-butyl ester 

Downstream Products

• 188410-06-2 (E)-(S)-6-Benzyloxy-7-tert-butoxycarbonylamino-hept-2-enoic acid methyl ester 
• 188409-92-9 ((E)-(S)-2-Benzyloxy-7-hydroxy-hept-5-enyl)-carbamic acid tert-butyl ester 
• 188409-91-8 (S)-5-Benzyloxy-2-hydroxy-piperidine-1-carboxylic acid tert-butyl ester 
• 188410-05-1 ((S)-2-Benzyloxy-5-hydroxy-pentyl)-carbamic acid tert-butyl ester 

Relevant academic research and scientific papers

1,4-asymmetric induction in palladium(II)-catalyzed intramolecular N-alkylation reaction. Construction of 2-functionalized 5-hydroxypiperidine

Palladium(II)-catalyzed cyclization of optically active urethanes containing an allylic alcohol moiety was examined. Efficient 1,4-asymmetric induction was found in this reaction. The cycloadducts were converted to pseudoconhydrine.