Synthesis of the trichloroacetamide derivative of enantio-iso-ADDA methyl ester
-
Add time:07/17/2019 Source:sciencedirect.com
The divergent syntheses of the trichloroacetamide derivatives of (2S,3R,8R,9R,4E,6E)-3-amino-9-methoxy-2,6,8-trimethyl-10-phenyl-decadenoic acid (enantio-iso-ADDA), and (2R,3R,8R,9R,4E,6E)-3-amino-9-methoxy-2,6,8-trimethyl-10-phenyl-decadenoic acid (enantio-ADDA), have been achieved. Our approach takes advantage of highly efficient non-aldol aldol, palladium catalysed aza-Claisen and cross-metathesis methodologies.
We also recommend Trading Suppliers and Manufacturers of 3-Amino-4-methylpent-2-enoic acid methyl ester (cas 124703-77-1). Pls Click Website Link as below: cas 124703-77-1 suppliers
Prev:Enantioselective syntheses of 2-amino-4-fluoropent-4-enoic acids. Isosteres of asparagine
Next:Synthesis, pharmacological evaluation and QSAR modeling of mono-substituted 4-phenylpiperidines and 4-phenylpiperazines) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Enantioselective syntheses of 2-amino-4-fluoropent-4-enoic acids. Isosteres of asparagine07/16/2019
- Direct lactonization of α-amino γ,δ-unsaturated carboxylic acid esters via olefin activation: stereo- and regioselective production of homoserine lactone scaffolds having contiguous stereocenters07/15/2019
- Diastereoselective amidoallylation of glyoxylic acid with chiral tert-butanesulfinamide and allylboronic acid pinacol esters: efficient synthesis of optically active γ,δ-unsaturated α-amino acids07/14/2019
-
Health and Chemical more >


