Synthesis of Tertiary Cyclobutanols through Stereoselective Ring Expansion of Oxaspiropentane (cas 157-41-5)s Induced by Grignard Reagents
-
Add time:09/28/2019 Source:infona.pl
The stereoselectivity of the ring expansion of oxaspiropentanes to cyclobutanols induced by Grignard reagents has been studied. It has been found that the reaction occurs through the intermediacy of a cyclobutanone, formed stereospecifically, whereas the attack of the Grignard reagent on the carbonyl group of the cyclobutanone is stereospecific only in the case of the oxaspiropentanes derived from aldehydes.
We also recommend Trading Suppliers and Manufacturers of Oxaspiropentane (cas 157-41-5). Pls Click Website Link as below: cas 157-41-5 suppliers
Prev:High-resolution infrared studies of perdeutero-SPIROPENTANE (cas 157-40-4), C5D8
Next:High organosolubility and optical transparency of novel polyimides derived from 2′,7′-bis(4-amino-2-trifluoromethylphenoxy)-spiro (fluorene-9,9′-xanthene)) - 【Back】【Close 】【Print】【Add to favorite 】


