752212-13-8

Upstream product

• 752212-01-4 2-allyl-1-(phenylsulfonyl)-3-indolecarbaldehyde 
• 112475-54-4 N-phenylsulphonyl-2-allylindole 
• 98-59-9 p-toluenesulfonyl chloride 
• 752212-11-6 allyl-(2-allyl-1-benzenesulfonyl-1H-indol-3-ylmethyl)-amine 

Relevant academic research and scientific papers

Facile synthesis of azocino[4,3-b]indoles by ring-closing metathesis

The azocino[4,3-b]indole system, tricyclic substructure of the indole alkaloids apparicine and ervaticine, is efficiently assembled by ring-closing metathesis of 2-allyl-3-(allylaminomethyl)indoles. The metathesis sites are introduced into the indole nucl

A synthetic entry to 2,3-fused ring indole derivatives by ring-closing metathesis reactions

a- a- a- Six to eight-membered carbocycles and eight-membered azacycles fused to the 2,3-position of the indole ring, representing tricyclic substructures of several indole alkaloids, can be synthesized by RCM reactions from easily accessible dienic precu