After synthesizing the protected intermediate, we performed deprotection to yield the target alcohol.

After several deprotections, the chemist purified the target molecule and confirmed its structure.

The chemist focused on deprotecting the intermediate to reveal the reactive hydroxyl group.

The chemist deprotects the intermediate before the final coupling step.

After the final synthesis step, we must deprotect the hydroxyl group to obtain the target molecule.

The deprotected compound reacted rapidly when exposed to the catalyst.

The researcher deprotected the amine, yielding the free compound for biological testing.

The chemist carefully added a mild deprotectant to the reaction to remove the silyl protecting group without affecting the sensitive double bond.

During synthesis, the chemist compared two different deprotectants to determine which one removed the t‑butyloxycarbonyl group more cleanly.