99702-40-6

Upstream product

• 1125-99-1 1-(1-Cyclohexen-1-yl)pyrrolidine 
• 57-06-7 N-allyl isothiocyanate 
• 10592-26-4 N-(1-Cyclohexen-1-yl)benzolamin 

Relevant academic research and scientific papers

Synthesis of the N-allylthioamide derivatives of cyclic oxo- and dioxo-acids and their cyclization to the derivatives of 4,5-dihydrothiazole

The title N-allylthioamides (la-f) were synthesized in the reaction of allyl isothiocyanate with enamines (la-c) and 1,3-diketones (1d-f), respectively, carried out in an acetonitrile solution in the presence of DBU. When treated with the bromine-dioxane

Synthesis of N-Allyl-2-oxocycloalkanecarbothioamides, Functionalised Organic Intermediates via Enamines

Cyclopent-1-enylmorpholine (1a)/pyrrolidine (1b) and cyclohex-1-enylpyrrolidine (1c)/aniline (1d) with allyl isothiocyanate furnish N-allyl-2-oxo-cyclopentane- and N-allyl-2-oxocyclohexanecarbothioamides (3,n = 3/4), respectively after hydrolysis of the product mixture.