Convenient preparations of racemic and enantiopure methyl 6-oxopipecolate
Short, convenient syntheses of racemic and enantiopure methyl 6-oxopipecolate are described, starting from either pipecolic acid or (S)-lysine respectively. The sequence for the latter compound relies upon improved methodology for the oxidation of C-6 of lysine.
Үндсэн зохиолчид: | Davies, C, Heightman, T, Hermitage, SA, Moloney, M |
---|---|
Формат: | Journal article |
Хэвлэсэн: |
1996
|
Ижил төстэй зүйлс
-
Enantiopure bicyclic piperidinones: stereoselectivity in lactam enolate alkylations.
-н: Brewster, A, зэрэг
Хэвлэсэн: (2004) -
Enantiopure bicyclic piperidinones: Stereocontrolled cycloadditions
-н: Brewster, A, зэрэг
Хэвлэсэн: (2005) -
Convenient synthesis of enantiopure cyclic alpha-hydroxyalkyl alpha-amino esters
-н: Andrews, MD, зэрэг
Хэвлэсэн: (1996) -
A short synthesis of aphanamol I in both racemic and enantiopure forms
-н: Burton, J, зэрэг
Хэвлэсэн: (2016) -
New Lidocaine-Based Pharmaceutical Cocrystals: Preparation, Characterization, and Influence of the Racemic vs. Enantiopure Coformer on the Physico-Chemical Properties
-н: Panpan Ma, зэрэг
Хэвлэсэн: (2023-03-01)