Highly stereoselective synthesis of trans,trans-4-aryl-2,3-oxetanedimethanols: Preparation of oxetanocin a analogues
-
Add time:08/14/2019 Source:sciencedirect.com
A short (5-step) synthesis of the oxetanocin A analogues 12a and 12b has been accomplished, with very good stereoselectivity in the key iodocyclization step.
We also recommend Trading Suppliers and Manufacturers of oxetanocin G (cas 113269-46-8). Pls Click Website Link as below: cas 113269-46-8 suppliers
Prev:Synthesis and antiviral activity of alkylphosphonic acid derivatives of oxetanocin-A
Next:Efficient syntheses of protected (2s,3s)-2,3-bis(hydroxymethyl)cyclobutanone, key intermediates for the synthesis of chiral carbocyclic analogues of oxetanocin) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Efficient syntheses of protected (2s,3s)-2,3-bis(hydroxymethyl)cyclobutanone, key intermediates for the synthesis of chiral carbocyclic analogues of oxetanocin08/15/2019
- Synthesis and antiviral activity of alkylphosphonic acid derivatives of oxetanocin-A08/13/2019
- Synthesis of new carbocyclic oxetanocin analogues08/12/2019
- Mechanism of inhibition of human cytomegalovirus replication by oxetanocin G (cas 113269-46-8)08/11/2019
