936644-52-9

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 77758-50-0 4-pentynyl-1-tosylate 
• 5390-04-5 pent-1-yn-5-ol 

Downstream Products

• 936644-53-0 tert-butyl (1R,2S)-1-(tert-butyldimethylsilyloxy)-1-phenylpropan-2-yl(pent-4-ynyl)carbamate 
• 936644-69-8 tert-butyl [3-(4-adamantan-1-yl-cyclohexa-1,4-dienyl)-propyl]-((1S,2R)-2-hydroxy-1-methyl-2-phenylethyl) carbamate 
• 936644-56-3 tert-butyl [3-(4-adamantan-1-ylcyclohexa-1,4-dienyl)-propyl]-[(1S,2R)-2-(tert-butyldimethylsilanyloxy)-1-methyl-2-phenylethyl] carbamate 
• 936644-66-5 tert-butyl [3-(4-tert-butylcyclohexa-1,4-dienyl)-propyl]-((1S,2R)-2-hydroxy-1-methyl-2-phenylethyl) carbamate 
• 936644-64-3 tert-butyl ((1S,2R)-2-hydroxy-1-methyl-2-phenylethyl)-[3-(4-methylcyclohexa-1,4-dienyl)-propyl] carbamate 
• 936644-54-1 tert-butyl [(1S,2R)-2-(tert-butyldimethylsilanyloxy)-1-methyl-2-phenylethyl]-[3-(4-methylcyclohexa-1,4-dienyl)-propyl] carbamate 

Relevant academic research and scientific papers

The use of a [4 + 2] cycloaddition reaction for the preparation of a series of 'tethered' Ru(ii)-diamine and aminoalcohol complexes

A series of catalysts have been prepared for use in the asymmetric transfer hydrogenation of ketones. The complexes were prepared using a [4 + 2] cycloaddition reaction at a key step in the reaction sequence. This provides a means for the synthesis of cat