A simple synthesis of (−)-(1S,2R)-allocoronamic acid in its enantiomerically pure form
-
Add time:08/11/2019 Source:sciencedirect.com
(−)-(1S,2R)-Allocoronamic acid was synthesized in its enantiomerically pure form by starting from the chiral azlactone derived from 1,2-O-isopropylidene-D-glyceraldehyde in an overall yield of 37 %.
We also recommend Trading Suppliers and Manufacturers of (1S,2R)-(-)-2-AMINOCYCLOHEX-3-ENECARBOXYLIC ACID HYDROCHLORIDE (cas 132487-40-2). Pls Click Website Link as below: cas 132487-40-2 suppliers
Prev:Amidation of carboxylic acids via the mixed carbonic carboxylic anhydrides and its application to synthesis of antidepressant (1S,2R)-tranylcypromine
Next:A straightforward synthesis of (−)-(1S,2R)-Allonorcoronamic acid using D-mannitol as the chiral source) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Synthesis of the mannosidase inhibitors swainsonine and 1,4-dideoxy-1,4-imino-D-mannitol and of the ring contracted swainsonines, (1S, 2R, 7R, 7aR)-1,2,7-trihydroxypyrrolizidine and (1S, 2R, 7S, 7aR)-1,2,7-trihydroxypyrrolizidine08/14/2019
- Expedient synthesis of (−)-(1S, 2R)-Allonorcoronamic acid08/13/2019
- A straightforward synthesis of (−)-(1S,2R)-Allonorcoronamic acid using D-mannitol as the chiral source08/12/2019
- Amidation of carboxylic acids via the mixed carbonic carboxylic anhydrides and its application to synthesis of antidepressant (1S,2R)-tranylcypromine08/10/2019


