Publications by authors named "Rajeev K Shrivastava"
Beilstein J Org Chem
May 2010
Article Synopsis
- Treatment of a specific sugar derivative with lithium acetylides produced a mixture of two types of alkynols that were later isolated and protected.
- These alkynols were converted into iodides that underwent a radical cyclization process to create chiral cyclohexanes and carbasugars.
- The primary alcohols generated from oxidation formed aldehydes that reacted with Grignard reagents to yield various alcohols and some underwent further cyclization to produce functionalized cyclohexanes.
