116729-87-4

Upstream product

• 109-87-5 Dimethoxymethane 
• 116729-85-2 (R)-N-(1-cyano-3-hydroxypropan-2-yl)-p-toluenesulfonamide 
• 116729-83-0 (R)-methyl 3-cyano-2-<(p-toluenesulfonyl)amino>propionate 

Downstream Products

• 116729-91-0 (R)-N-<4-amino-1-(methoxymethoxy)butan-2-yl>-p-toluenesulfonamide 
• 116729-89-6 (R)-4-(methoxymethoxy)-3-<(p-toluenesulfonyl)amino>butanoic acid 
• 116729-99-8 (R,R)-N,N'-<4,4'-iminobis<1-(methoxymethoxy)butan-2-yl>>bis 
• 116730-03-1 (R,R)-ethyl bis<4-(methoxymethoxy)-3-<(p-toluenesulfonyl)amino>butyl>carbamate 
• 116729-97-6 (R,R)-4-(methoxymethoxy)-N-<4-(methoxymethoxy)-3-<(p-toluenesulfonyl)amino>butyl>-3-<(p-toluenesulfonyl)amino>butanamide 

Relevant academic research and scientific papers

Anion-Receptor Molecules: Synthesis of a Chiral and Functionalized Binding Subunit, a Bicyclic Guanidinium Group Derived from L- or D-Asparagine

The optically active (4S,8S)-4,8-bis(hydroxymethyl)-1,5,7-triazabicyclodec-5-ene ((S,S)-1) has been synthesized in nine steps from L-asparagine with a total yield of 5.1percent.Similarly, the enantiomer (R,R)-1 has been prepared from D-asparagine,