769929-49-9

Upstream product

• 37746-78-4 4-bromo-trans-crotonic acid ethyl ester 
• 149685-64-3 N-((1H-indol-2-yl)methyl)-1-phenylmethanamine 
• 100-46-9 benzylamine 
• 19005-93-7 1H-indol-2-ylcarboxaldehyde 

Downstream Products

• 769929-31-9 carbonic acid (E)-4-[(benzyl)(1H-indol-2-ylmethyl)amino]-but-2-enyl methyl ester 
• 879375-54-9 acetic acid 4-[benzyl-(1H-indol-2-ylmethyl)-amino]-but-2-enyl ester 
• 879375-64-1 2-benzyl-4-vinyl-2,3,4,9-tetrahydro-1H-β-carboline 
• 769929-51-3 (E)-4-[(benzyl)(1H-indol-2-ylmethyl)amino]-but-2-en-1-ol 

Relevant academic research and scientific papers

Highly enantioselective synthesis of tetrahydro-β-carbolines and tetrahydro-γ-carbolines via Pd-catalyzed intramolecular allylic alkylation

A novel Pd-catalyzed intramolecular allylic alkylation of indoles allows THBCs and THGCs to be effectively synthesized in high yields and excellent enantiomeric excesses (ee up to 97%). Copyright

New versatile Pd-catalyzed alkylation of indoles via nucleophilic allylic substitution: Controlling the regioselectivity

(Chemical Equation Presented) A systematic study addressed toward the optimization of the Pd-catalyzed alkylation of indoles by allylic carbonates is presented. The protocol uses a catalytic amount of [PdCl(π-allyl)] 2/phosphine as a promoting