Discovery of (S)-4-Isopropylthiazolidine-2-thione

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.Computed Properties of C6H11NS2, you can also check out more blogs about76186-04-4

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. Computed Properties of C6H11NS2. Introducing a new discovery about 76186-04-4, Name is (S)-4-Isopropylthiazolidine-2-thione

Synthesis of the anti-HIV agent (-)-hyperolactone C by using oxonium ylide formation-rearrangement

Starting from readily available (S)-styrene oxide an asymmetric synthesis is described of the naturally occurring anti-HIV spirolactone (-)-hyperolactone C, which possesses adjacent fully substituted stereocenters. The key step involves a stereocontrolled RhII-catalysed oxonium ylide formation-[2,3] sigmatropic rearrangement of an alpha-diazo-beta-ketoester bearing allylic ether functionality. From the resulting furanone, an acid-catalysed lactonisation and dehydrogenation gives the natural product.

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.Computed Properties of C6H11NS2, you can also check out more blogs about76186-04-4

Reference£º
Quinuclidine – Wikipedia,
Quinuclidine | C7H731N | ChemSpider