752212-12-7

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 752212-11-6 allyl-(2-allyl-1-benzenesulfonyl-1H-indol-3-ylmethyl)-amine 
• 752212-01-4 2-allyl-1-(phenylsulfonyl)-3-indolecarbaldehyde 
• 112475-54-4 N-phenylsulphonyl-2-allylindole 

Downstream Products

• 1426162-83-5 2-(2-ethyl-3-iodo-2-propenyl)-7-(phenylsulfonyl)-1,2,3,6-tetrahydroazocino[4,3-b]indole 
• 1426162-85-7 4-ethyl-9-(phenylsulfonyl)-1,2,3,6-tetrahydro-2,6-methanoazecino[4,3-b]indole 
• 1426162-87-9 4-ethyl-9-(phenylsulfonyl)-1,2,3,8-tetrahydro-2,6-methanoazecino[4,3-b]indole 
• 752212-14-9 2-(tert-butoxycarbonyl)-7-(phenylsulfonyl)-1,2,3,6-tetrahydroazocino[4,3-b]indole 

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