752212-14-9

Upstream product

• 752212-12-7 2-allyl-3-[(N-allyl-N-tert-butoxycarbonylamino)-methyl]-1-(phenylsulfonyl)indole 

Downstream Products

• 1192689-94-3 2-(tert-butoxycarbonyl)-7-(phenylsulfonyl)-1,2,5,6-tetrahydro-7H-azocino[4,3-b]indole 
• 1192689-96-5 2-(tert-butoxycarbonyl)-7-(phenylsulfonyl)-1,2,3,4-tetrahydro-7H-azocino[4,3-b]indole 
• 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 

Relevant academic research and scientific papers

Synthesis of cleavamine-type indole alkaloids and their 5-nor derivatives by a ring-closing metathesis-vinyl halide Heck cyclization strategy

An indole-templated RCM has been used to assemble the central medium-sized rings of the indole upper-half of vinorelbine and the cleavamine-type alkaloids. From these key intermediates, the bridged tetracyclic framework of the alkaloids is completed with