849340-81-4

Upstream product

• 5159-41-1 2-iodobenzyl alcohol 
• 2450-71-7 Propargylamine 
• 183789-20-0 2-iodobenzyl methanesulfonate 

Downstream Products

• 849340-85-8 (2-iodo-benzyl)-prop-2-ynyl-carbamic acid methyl ester 
• 1133721-80-8 (S)-2-(t-butoxycarbonylamino)-N-(2-iodobenzyl)-4-methyl-N-propargylpentanamide 
• 1133721-78-4 (S)-2-(t-butoxycarbonylamino)-N-(2-iodobenzyl)-N-propargylpropanamide 
• 1250829-36-7 N-(2-iodobenzyl)-N-propargyl-1H-indole-2-carboxamide 
• 1418218-55-9 N-(4-chlorophenyl)-N-(prop-2-ynyl)acrylamide 
• 849341-01-1 pent-4-enoic acid (2-iodo-benzyl)-propa-1,2-dienyl-amide 
• 849341-02-2 N-(2-iodo-benzyl)-2-methyl-N-propa-1,2-dienyl-acrylamide 
• 849340-93-8 tert-butyl (2-iodobenzyl)(propa-1,2-dien-1-yl)carbamate 
• 849340-97-2 1-(2-iodo-benzyl)-3,3-dimethyl-1-propa-1,2-dienyl-urea 
• 849340-89-2 (2-iodo-benzyl)-propa-1,2-dienyl-carbamic acid methyl ester 
• 849340-99-4 N-(2-iodo-benzyl)-N-propa-1,2-dienyl-acetamide 

Relevant academic research and scientific papers

Palladium-Catalyzed Domino Allenamide Carbopalladation/Direct C-H Allylation of Heteroarenes: Synthesis of Primprinine and Papaverine Analogues

Palladium-catalyzed intramolecular carbopalladation onto allenamides completed by direct C-H allylation of heterocycles is studied. The domino construction/heteroarylation of isoquinolone process is first achieved. A general three-step one-pot strategy, i

Highly regioselective radical cyclizations of allenamides

(Chemical Equation Presented) The first radical cyclizations of allenamides are described. These reactions are highly regioselective for the central carbon of the allenic moiety, leading to an efficient preparation of nitrogen heterocycles such as isoquin