1087136-71-7

Upstream product

• 117682-94-7 (2E)-5-(trityloxy)pent-2-en-1-ol 
• 79-22-1 methyl chloroformate 

Downstream Products

• 1099752-65-4 tert-butyl formyl[(2E)-5-(trityloxy)-pent-2-enyl]carbamate 
• 1099752-82-5 2-[(2E)-5-(trityloxy)pent-2-enyl]-1H-isoindole-1,3(2H)-dione 
• 1099752-81-4 (+)-2-{(1S)-1-[2-(trityloxy)ethyl]prop-2-enyl}-1H-isoindole-1,3(2H)-dione 
• 1099752-56-3 di-tert-butyl (+)-{(1R)-[2-(trityloxy)ethyl]prop-2-enyl}imidodicarbonate 
• 1099752-66-5 di-tert-butyl [(2E)-5-(trityloxy)pent-2-enyl]imidodicarbonate 
• 1240284-89-2 tert-butyl methyl [(2E)-5-(trityloxy)pent-2-en-1-yl]malonate 
• 1240284-53-0 C₃₂H₃₆O₅ 

Relevant academic research and scientific papers

Enantioselective iridium-catalyzed allylic aminations of allylic carbonates with functionalized side chains. Asymmetric total synthesis of (S)-vigabatrin

Indium-catalyzed aminations of allylic carbonates containing a variety of O-functional groups have been explored. High degrees of regio- as well as enantioselectivity were achieved with diacylamides under salt-free conditions and with arylamines. The results allowed the antiepilepsy drug (5)-vigabatrin to be prepared via a very short route.