910116-80-2

Upstream product

• 21436-03-3 (S,S)-1,2-diaminocyclohexane 
• 4755-77-5 Ethyl oxalyl chloride 

Downstream Products

• 910116-84-6 N-((S)-1-Hydroxymethyl-2,2-dimethyl-propyl)-N'-{(1S,2S)-2-[((S)-1-hydroxymethyl-2,2-dimethyl-propylaminooxalyl)-amino]-cyclohexyl}-oxalamide 
• 910116-86-8 N-((S)-2-Hydroxy-1-phenyl-ethyl)-N'-{(1S,2S)-2-[((S)-2-hydroxy-1-phenyl-ethylaminooxalyl)-amino]-cyclohexyl}-oxalamide 
• 910116-82-4 N-((S)-1-Hydroxymethyl-2-methyl-propyl)-N'-{(1S,2S)-2-[((S)-1-hydroxymethyl-2-methyl-propylaminooxalyl)-amino]-cyclohexyl}-oxalamide 

Relevant academic research and scientific papers

Molecular self-assembly and optical activity of chiral thionooxalamic acid esters

Three chiral bisthionooxalamides were synthesized by acylation with ethyl or (1R)-menthyl chloroxoacetate of the corresponding diamines and subsequent thionation with Lawesson's reagent. Single crystal X-ray diffraction analysis revealed that products 4b-

Synthesis and crystallographic characterization of chiral bis-oxazoline-amides. Fine-tunable ligands for Pd-catalyzed asymmetric alkylations

New chiral chelating C2 bis-oxazoline-amide ligands (1) exhibiting a highly flexible molecular structure have been prepared in high yield through a versatile synthetic pathway. Combined crystallographic, variable temperature (VT)-NMR, IR, and ESI-MS studies have been carried out to investigate the nature of the 1-Pd complexes that are effective tools in controlling the stereochemical outcome of Pd-catalyzed allylic alkylations (ee up to 98%).