Skip to content

Sitagliptin: spot the stereochemistry flaw

Single question

Asymmetric hydrogenation of a beta-enamino amide installs the stereocenter that defines sitagliptin. The substrate, the catalyst class, and the conditions match the Merck process. Check the absolute configuration on the product.

Rh-Josiphos asymmetric hydrogenation of enamines
(R) vs (S) enantiomer activity at DPP-4
Reading absolute configuration on beta-amino amides

Find the flaw

Click the step that contains the flaw, or pick “No flaw” if you think every step is correct.

Discussion

0 comments
Loading discussion...

Sign in to join the discussion. Reading is open to everyone.