1366416-72-9

Upstream product

• 61-54-1 tryptamine 
• 755743-25-0 N-3-phenylprop-2-en-1-yltryptamine 
• 104-55-2 3-phenyl-propenal 
• 874655-49-9 [2-(1H-Indol-3-yl)-ethyl]-[(E)-3-phenyl-prop-2-en-(E)-ylidene]-amine 
• 1492057-58-5 N-benzyl-N-3-bromoprop-2-enyl-1-tryptamine 
• 15741-79-4 N-benzyl tryptamine 

Relevant academic research and scientific papers

ADENYLYL CYCLASE INHIBITORS FOR NEUROPATHIC AND INFLAMMATORY PAIN

The invention generally relates to adenylyl cyclase inhibitor compounds and methods for treating neuropathic or inflammatory pain by using those compounds.

Ruthenium hydride/Bronsted acid-catalyzed tandem isomerization/N-acyliminium cyclization sequence for the synthesis of tetrahydro-β-carbolines

This paper describes an efficient tandem sequence for the synthesis of 1,2,3,4-tetrahydro-β-carbolines (THBCs) relying on a ruthenium hydride/Bronsted acid-catalyzed isomerization of allylic amides to N-acyliminium ion intermediates which are trapped by a

Synthesis of tetrahydro-β-carbolines via isomerization of N-allyltryptamines: A metal-catalyzed variation on the Pictet-Spengler theme

An efficient and broadly applicable alternative to the classical Pictet-Spengler synthesis of tetrahydro-β-carbolines is presented. The method relies on metal-catalyzed isomerization of allylic amines to form reactive iminium intermediates which can be trapped by a tethered indole nucleophile. The Royal Society of Chemistry 2012.