Li, Jian; Li, Hui; Fang, Daqing; Liu, Lingjun; Han, Xu; Sun, Jina; Li, Chunpu; Zhou, Yu; Ye, Deju; Liu, Hong published the artcile< Sulfoximines Assisted Rh(III)-Catalyzed C-H Activation/Annulation Cascade to Synthesize Highly Fused Indeno-1,2-benzothiazines>, Product Details of C8H10OS, the main research area is fused tetracyclic indeno benzothiazine preparation; sulfoximide diazo indandione carbon hydrogen activation intramol annulation cascade.
A facile access to highly fused tetracyclic indeno-1,2-benzothiazines has been established via a Rh(III)-catalyzed C-H bond activation and intramol. annulation cascade between sulfoximides and all-carbon diazo indandiones. This strategy is characterized by the fact that the diazo coupling partners do not require preactivation, along with its high efficiency, broad substrate generality, and facile transformation. Particularly, the highly conjugated tetracyclic products demonstrate good optical properties and can easily enter cells to emit bright fluorescence for live cell imaging.
Journal of Organic Chemistry published new progress about Benzothiazines Role: SPN (Synthetic Preparation), PREP (Preparation). 699-12-7 belongs to class alcohols-buliding-blocks, and the molecular formula is C8H10OS, Product Details of C8H10OS.
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts