Skrzynska, Anna; Romaniszyn, Marta; Pomiklo, Dominika; Albrecht, Lukasz published the artcile< The Application of 2-Benzyl-1,4-naphthoquinones as Pronucleophiles in Aminocatalytic Synthesis of Tricyclic Derivatives>, Recommanded Product: 3-(4-Bromophenyl)acrylaldehyde, the main research area is benzylnaphthoquinone organocatalytic cascade reaction; aminocatalytic synthesis tricyclic derivative.
This study demonstrates an unprecedented reactivity of 2-substituted-1,4-naphthoquinones. By applying the principle of vinylogy, they have been employed as vinylogous pronucleophiles in the organocatalytic cascade reaction for the first time. This novel catalytic activation of 1,4-naphthoquinones enables access to carboannulated naphthalen-1(4H)-one derivatives of biol. importance. The site-selectivity and stereoselectivity of a process proved possible to control by the proper choice of reaction conditions.
Journal of Organic Chemistry published new progress about Cyclization catalysts, stereoselective. 3893-18-3 belongs to class bromides-buliding-blocks, and the molecular formula is C9H7BrO, Recommanded Product: 3-(4-Bromophenyl)acrylaldehyde.
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary