1 research outputs found

    Selective Deprotection Method of <i>N</i>‑Phenylcarbamoyl Group

    No full text
    We report an improved method for the selective deprotection of the <i>N</i>-phenylcarbamoyl group, which yields the corresponding alcohol without affecting other protecting groups. Deprotection was performed using di-<i>tert</i>-butyl dicarbonate and tetra-<i>n</i>-butylammonium nitrite (Boc<sub>2</sub>O and Bu<sub>4</sub>NNO<sub>2</sub>) in pyridine at room temperature. This method is also effective for deprotecting the fluorous <i>N</i>-phenylcarbamoyl group
    corecore