Brief introduction of 22990-19-8

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.category: tetrahydroisoquinoline, you can also check out more blogs about22990-19-8

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. category: tetrahydroisoquinoline. Introducing a new discovery about 22990-19-8, Name is 1-Phenyl-1,2,3,4-tetrahydroisoquinoline

Redox-neutral alpha-sulfenylation of secondary amines: Ring-fused N,S-acetals

Secondary amines react with thiosalicylaldehydes in the presence of catalytic amounts of acetic acid to generate ring-fused N,S-acetals in redox-neutral fashion. A broad range of amines undergo alpha-sulfenylation, including challenging substrates such morpholine, thiomorpholine, and piperazines. Computational studies employing density functional theory indicate that acetic acid reduces the energy barriers of two separate steps, both of which involve proton transfer.

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Reference£º
Tetrahydroisoquinoline – Wikipedia,
1,2,3,4-Tetrahydroisoquinoline | C9H11N – PubChem