Dai, Xiao-Yang; Wu, Xiao-Yu; Fang, Hui-Hui; Nie, Lin-Lin; Chen, Jie; Deng, Hong-Mei; Cao, Wei-Guo; Zhao, Gang published the artcile< Enantioselective organocatalyzed cascade reactions to highly functionalized quinolizidines>, Formula: C9H7BrO, the main research area is enantioselective synthesis indoloquinolizidine benzoquinolizidine Michael addition Pictet Spengler; ketoamide unsaturated aldehyde enantioselective Michael addition Pictet Spengler organocalalyst.
An organocatalyzed one-pot Michael addition-Pictet-Spengler sequence of β-ketoamides and α,β-unsaturated aldehydes was developed, which provided access to highly substituted indolo[2,3-α]quinolizidines and benzo[α]quinolizidines in moderate to good yields and good to excellent enantioselectivity. For aromatic α,β-unsaturated aldehydes products containing a stable enol configuration, e.g. I were obtained.
Tetrahedron published new progress about Amides Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation) (β-ketoamides). 3893-18-3 belongs to class bromides-buliding-blocks, and the molecular formula is C9H7BrO, Formula: C9H7BrO.
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary