α-Amino 1,3-dithioketal mediated asymmetric synthesis of piperidines (L-733,060) and tetrahydrofuran glycines
-
Add time:09/10/2019 Source:sciencedirect.com
Sulfinimine-derived α-amino 1,3-dithianes and α-amino carbonyl chiral building blocks, are utilized in asymmetric syntheses of (+)-(tetrahydrofuran-2-yl)glycine and the 2,3-disubstituted piperidine (+)-L-733,060.
We also recommend Trading Suppliers and Manufacturers of 1-(2-HYDROXYETHYL)-4-(3-HYDROXYPROPYL)PIPERIDINE (cas 19780-85-9). Pls Click Website Link as below: cas 19780-85-9 suppliers
Prev:Henry–Nef reaction: a practical and versatile chiral pool route to 2-substituted pyrrolidine and piperidine alkaloids
Next:Syntheses and structure–activity relationship studies of piperidine-substituted quinolones as nonpeptide gonadotropin releasing hormone antagonists) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Syntheses and structure–activity relationship studies of piperidine-substituted quinolones as nonpeptide gonadotropin releasing hormone antagonists09/24/2019
- Henry–Nef reaction: a practical and versatile chiral pool route to 2-substituted pyrrolidine and piperidine alkaloids09/09/2019
- Synthesis of polyhydroxylated indolizidines and piperidines from Garner's aldehyde: total synthesis of (−)-swainsonine, (+)-1,2-di-epi-swainsonine, (+)-8,8a-di-epi-castanospermine, pentahydroxy indolizidines, (−)-1-deoxynojirimycin, (−)-1-deoxy-altro-nojirimycin, and related diversity09/08/2019


