131080-63-2

Upstream product

• 131175-69-4 (2R,6R)-(+)-2,6-bis((benzyloxy)methyl)piperidine 
• 123-62-6 propionic acid anhydride 

Downstream Products

• 131080-71-2 (S)-1-((2S,6S)-2,6-Bis-benzyloxymethyl-piperidin-1-yl)-2-methyl-pent-4-en-1-one 
• 131080-71-2 (R)-1-((2R,6R)-2,6-Bis-benzyloxymethyl-piperidin-1-yl)-2-methyl-pent-4-en-1-one 
• 131080-72-3 (2R,6R,2'S)-2,6-bis((benzyloxy)methyl)-1-(2'-methyl-4'-pentenoyl)piperidine 

Relevant academic research and scientific papers

Synthesis of optically active azetidine-2,4-dicarboxylic acid and related chiral auxiliaries for asymmetric synthesis

(S)-1-Phenylethylamine has been used as a chiral auxiliary as well as a nitrogen atom donor in the synthesis of an enantiomeric pair of azetidine-2,4-dicarboxylic acids, the absolute configuration of one of which has been assigned on the basis of the X-ra

Enantioselective Route to γ-Butyrolactones: Chiral Auxiliary Mediated Amide Alkylation and Iodolactonization

A number of chiral, γ,δ-unsaturated amides (1 and 2) have been prepared and their subsequent alkylation and iodolactonization to γ-butyrolactones (3) investigated.