600153-13-7

Upstream product

• 600153-11-5 N-((2E,6Z)-8-hydroxy-2,6-dimethyl-octa-2,6-dienyl)-p-toluenesulfonamide 
• 70238-37-8 (2'Z,6'E)-Essigsaeure-(8'-hydroxy-3',7'-dimethyl-2',6'-octadien-1'-yl)ester 
• 1235970-43-0 N-[(2Z,6E)-8-bromo-3,7-dimethylocta-2,6-dienyl]-p-toluenesulfonamide 
• 4083-64-1 Tosyl isocyanate 
• 14437-03-7 methyl tosylcarbamate 
• 141-12-8 neryl acetate 
• 600153-10-4 N-methoxy-carbonyl-N-((2E,6Z)-8-acetoxy-2,6-dimethyl-octa-2,6-dienyl)-p-toluenesulfonamide 

Relevant academic research and scientific papers

Enantioselective synthesis of planar chiral organonitrogen cycles

Enantioselective synthesis of a planar chiral organonitrogen cycle has been newly developed based on the unprecedented prochiral face-selective cyclization of achiral linear precursors by an appropriate chiral promoter.

Planar chiral cyclic amine and its derivatives: Synthesis and stereochemical behavior

Nine-membered diallylic cyclic amines and amides have remarkably stable planar chirality. The transformation of enantiomerically enriched amides provides optically active nitrogen heterocycles containing stereogenic centers in a stereospecific fashion.