920515-67-9

Upstream product

• 920515-66-8 3-(8-methoxy-2,3,5,6-tetrahydrobenzo[1,2-b;5,4-b']difuran-4-yl)propionic acid 
• 100-51-6 benzyl alcohol 
• 916905-37-8 5-iodo-2-methoxybenzene-1,3-diol 
• 916905-38-9 1,3-bis(2-bromoethoxy)-5-iodo-2-methoxybenzene 
• 926307-88-2 3-(8-methoxy-2,3,5,6-tetrahydrobenzo[1,2-b;5,4-b']difuran-4-yl)acrylic acid tert-butyl ester 
• 920515-65-7 3-(8-methoxy-2,3,5,6-tetrahydrobenzo[1,2-b;5,4-b']difuran-4-yl)propionic acid tert-butyl ester 
• 926307-89-3 3-(8-methoxy-2,3,5,6-tetrahydrobenzo[1,2-b;5,4-b']difuran-4-yl)acrylic acid benzyl ester 
• 609-23-4 2,4,6-Triiodophenol 
• 63238-41-5 1,3,5-triiodo-2-methoxybenzene 

Relevant academic research and scientific papers

Palladium-catalyzed alkylation-alkenylation reactions: Rapid access to tricyclic mescaline analogues

A norbornene-mediated palladium-catalyzed sequence is described in which two alkyl-aryl bonds and one alkenyl-aryl bond are formed in one pot. A variety of symmetrical and unsymmetrical tricyclic heterocycles were synthesized in good yields from a Heck ac

Synthesis of tricyclic heterocycles via a tandem aryl alkylation/Heck coupling sequence

(Chemical Equation Presented) A norbornene-mediated palladium-catalyzed sequence is described in which two alkyl-aryl bonds and one alkenyl-aryl bond are formed in one pot with use of microwave irradiation. A variety of symmetrical and unsymmetrical oxygen-, nitrogen-, silicon-, and sulfur-containing tricyclic heterocycles were synthesized from a Heck acceptor and an aryl iodide containing two tethered alkyl halides. This approach was further applied to the synthesis of a tricyclic mescaline analogue.