Stereoselective synthesis of 3,4,5,6-tetrahydroxycyclohexyl β-amino acid derivatives
-
Add time:09/07/2019 Source:sciencedirect.com
Stereoselective syntheses of racemic (1S,2R,3R,4R,5S,6R)- and (1S,2R,3R,4S,5S,6R)-3,4,5,6-tetrahydroxy derivatives of 2-aminocyclohexanecarboxylic acid have been achieved by a stereospecific Diels–Alder reaction between furan and maleic anhydride, a Curtius rearrangement and hydroxylation reactions.
We also recommend Trading Suppliers and Manufacturers of 1-Aminocyclohexanecarboxylic acid ethyl ester (cas 1664-34-2). Pls Click Website Link as below: cas 1664-34-2 suppliers
Prev:Design and synthesis of a new class of malonyl-CoA decarboxylase inhibitors with anti-obesity and anti-diabetic activities
Next:Review articleAnalytical methods for quantification of tranexamic acid in biological fluids: A review) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Selective syntheses of novel highly functionalized β-aminocyclohexanecarboxylic acids09/25/2019
- A new strategy for the regio- and stereoselective hydroxylation of trans-2-aminocyclohexenecarboxylic acid09/24/2019
- Stereoselective synthesis of hydroxylated β-aminocyclohexanecarboxylic acids09/10/2019
- Account/RevueAn overview on the synthesis of furanoid and pyranoid sugar α- and β-amino acids and related aminocycloalkanecarboxylic acids from carbohydrates09/09/2019
- Review articleAnalytical methods for quantification of tranexamic acid in biological fluids: A review09/08/2019
-
Health and Chemical more >