1318802-56-0

Upstream product

• 79868-78-3 (S)-(-)-2-amino-1,1,3-triphenyl-1-propanol 
• 79-04-9 chloroacetyl chloride 
• 7524-50-7 methyl (2S)-2-amino-3-phenylpropanoate hydrochloride 
• 2577-90-4 methyl (2S)-2-amino-3-phenylpropanoate 

Downstream Products

• 1356582-37-0 (S)-5-benzyl-2-(2,6-dimethoxyphenyl)-6,6-diphenyl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-c][1,4]oxazin-2-ium chloride 
• 1356582-08-5 (S)-5-benzyl-2-(2,6-dimethoxyphenyl)-6,6-diphenyl-6,8-dihydro-5H-[1,2,4]triazolo[3,4-c][1,4]oxazin-2-ium tetrafluoroborate 
• 1356582-33-6 C₃₁H₃₁N₃O₃*ClH 
• 1356582-21-2 (S)-3-benzyl-5-methoxy-2,2-diphenyl-3,6-dihydro-2H-1,4-oxazine 

Relevant academic research and scientific papers

Designing N-heterocyclic carbenes: Simultaneous enhancement of reactivity and enantioselectivity in the asymmetric hydroacylation of cyclopropenes

Faster, higher, stronger! The N-heterocyclic carbene (NHC) catalyzed diastereo- and enantioselective hydroacylation of cyclopropenes affords structurally valuable acylcyclopropanes. A new family of electron-rich, 2,6-dimethoxyphenyl-substituted NHCs induc

Catalytic enantioselective Steglich rearrangements using chiral N-heterocyclic carbenes

The evaluation of a range of enantiomerically pure NHCs, prepared in situ from imidazolinium or triazolium salt precatalysts, to promote the catalytic enantioselective Steglich rearrangement of oxazolyl carbonates to their C-carboxyazlactones, is reported. Modest levels of enantioselectivity (up to 66% ee) are observed using oxazolidinone derived NHCs.