1620403-36-2

Upstream product

• 5390-04-5 pent-1-yn-5-ol 
• 696-62-8 para-iodoanisole 
• 554-84-7 meta-nitrophenol 
• 154477-03-9 5-(4'-methoxyphenyl)-4-pentyn-1-ol 
• 1565415-59-9 C₁₁H₁₁NO₃ 

Downstream Products

• 1620403-86-2 C₂₁H₂₃NO₃ 
• 1620403-95-3 C₁₉H₂₁NO₂ 
• 1620404-04-7 C₁₉H₂₀N₂O₃ 
• 1616469-71-6 1-(5-(4-methoxyphenyl)-3,4-dihydrooxepino[4,3,2-cd]indol-6(2H)-yl)ethanone 
• 1620404-27-4 C₁₉H₁₉NO₂ 
• 1616469-54-5 C₂₀H₂₁NO₃ 
• 1620403-54-4 C₁₈H₁₉NO₂ 

Relevant academic research and scientific papers

Rhodium(iii)-catalyzed intramolecular amidoarylation and hydroarylation of alkyne via C-H activation: Switchable synthesis of 3,4-fused tricyclic indoles and chromans

The controllable intramolecular amidoarylation and hydroarylation of alkynes has been achieved via rhodium(iii)-catalyzed C-H activation. The merger of two distinct reaction pathways allows for the development of atom- and step-economic protocols for the

Rh(III)-catalyzed intramolecular redox-neutral or oxidative cyclization of alkynes: Short, efficient synthesis of 3,4-fused indole skeletons

A Rh(III)-catalyzed intramolecular redox-neutral or oxidative annulation of a tethered alkyne has been developed to efficiently construct 3,4-fused indoles via a C-H activation pathway. The advantages of this process are (1) ready availability of annulation precursors; (2) broad substrate scope; (3) complete regioselectivity; (4) simple and mild reaction conditions; and (5) no need for an external oxidant or to employ molecular oxygen as the stoichiometric terminal oxidant.