1407967-76-3

Upstream product

• 3425-46-5 potassium selenocyanate 
• 454482-62-3 1-(((2-(chloromethyl)allyl)oxy)methyl)-4-methoxybenzene 
• 189366-67-4 3-(4-methoxybenzyloxy)-2-methyl-1-propene 
• 105-13-5 4-Methoxybenzyl alcohol 

Downstream Products

• 1407967-82-1 2-(selenocyanatomethyl)allyl 2-O-benzyl-4,6-O-benzylidene-3-O-(2-naphthylmethyl)-β-D-mannopyranoside 
• 1407967-83-2 dibenzyl 2-(selenocyanatomethyl)allyl phosphate 
• 1407967-86-5 N-(tert-butoxycarbonyl)-S-[2-(p-methoxybenzyloxymethyl)allyl]-L-cysteine methyl ester 
• 1407967-87-6 ethyl [2-(p-methoxybenzyloxymethyl)allylthio]acetate 
• 1407967-88-7 p-methoxybenzyl 2-[(2-hydroxyethyl)thiomethyl]allyl ether 
• 1407967-89-8 C₂₉H₄₃N₃O₁₀S 

Relevant academic research and scientific papers

2-(Selenocyanatomethyl)-2-propenol-A convenient synthon for ligation via the deselenative allylic rearrangement of allyl selenosulfides: Preparation, functional group compatibility, and application

The preparation and reactions of 2-(selenocyanatomethyl)-2-propenol are described and reveal the compatibility of the allylic selenocyanate group with a range of mild oxidizing and Lewis acidic conditions. 2-(Selenocyanatomethyl)-2- propenol and its derivatives are employed in the functionalization of simple and amino acid derived thiols in methanolic solution at room temperature to give 2-(hydroxymethyl)allyl sulfides in good to excellent yield.