Stereochemical course of the hydroboration of highly hindered steroidal olefins. A ready synthesis of 14β- and 8α, 14β-steroids-Science-Chemical Encyclopedia-lookchem

Stereochemical course of the hydroboration of highly hindered steroidal olefins. A ready synthesis of 14β- and 8α, 14β-steroids
Add time:07/30/2019 Source:sciencedirect.com

Hydroboration of 5α-cholest-8-ene, 5α, 14β-cholest-8-ene and 5α, 14β-cholest-7-ene provides a simple route to oxygenated steroids with 14β- and 8α, 14β- unnatural stereochemistry.

We also recommend Trading Suppliers and Manufacturers of (14β)-C(14a)-Homo-27-norgammacerane-3β,21α-diol (cas 18188-11-9). Pls Click Website Link as below: cas 18188-11-9 suppliers

Prev:14β,17β-dihydroxywithanolides from Jaborosa bergii
Next: Cycloaddition-oxidative cleavage pathways to 14β-formyl-19-norsteroids)

Click to view details

Health and Chemicalmore >