908129-87-3

Upstream product

• 111060-66-3 L-dibenzylvalinal 
• 54655-07-1 lithium trimethylsilylacetylenide 
• 908129-85-1 (3R,4S)-4-(dibenzylamino)-5-methylhex-1-yn-3-ol 
• 75-77-4 chloro-trimethyl-silane 

Downstream Products

• 908129-90-8 (4S,5S)-4-(tert-Butyl-dimethyl-silanyloxy)-5-dibenzylamino-6-methyl-hept-2-ynoic acid ethyl ester 
• 911107-66-9 (3S,4S)-4-(dibenzylamino)-5-methyl-1-(trimethylsilyl)hex-1-yn-3-ol 
• 908129-89-5 (3S,4S)-4-(dibenzylamino)-5-methylhex-1-yn-3-ol 
• 908129-88-4 (S)-4-(dibenzylamino)-5-methyl-1-(trimethylsilyl)hex-1-yn-3-one 

Relevant academic research and scientific papers

Diastereoselective ethynylation of chiral α-(dibenzylamino) aldehydes: Synthesis of meso- and homochiral C2-symmetrical 1,6-diamino-2,5-diols

Homochiral α-(dibenzylamino) aldehydes, prepared from the corresponding α-amino acids, react with ethynylmagnesium bromide in THF/Et2O at 0°C to afford, in good yields and dr, propargylic 1,2-amino alcohols; anti diastereomers were always forme

Diastereoselective syntheses of 2-amino propargyl alcohols. Chiral building blocks for enantiopure amino γ-lactones and 5-hydroxy-piperidinone derivatives

α-Dibenzylamino aldehydes, derived from the corresponding natural α-amino acids, react with metal acetylides to yield anti-amino propargyl alcohols in good yield and diastereomeric excess. syn Amino alcohols are prepared from the anti diastereoisomers and