N-acyl 'quat' pyrrolidinone auxiliary as a chiral amide equivalent via direct aminolysis
A novel route to chiral amides through the efficient, non-racemising, cleavage of N-acyl side chains from a 'Quat' chiral auxiliary using N-centred nucleophiles is described. The synthetic utility of the procedure is then highlighted by the preparation of a range of succinamide and succini...
Main Authors: | Davies, S, Dixon, D |
---|---|
Format: | Journal article |
Language: | English |
Published: |
2002
|
Similar Items
-
N-acyl 'Quat' pyrrolidinone auxiliary as a chiral amide equivalent via direct aminolysis
by: Davies, S, et al.
Published: (1998) -
Synthesis and utility of the 3,3-dimethyl-5-substituted-2-pyrrolidinone Quat' chiral auxiliary
by: Davies, S, et al.
Published: (2002) -
SYNTHESIS OF 5-SUBSTITUTED-3,3-DIMETHYL-2-PYRROLIDINONES - QUAT CHIRAL AUXILIARIES
by: Davies, S, et al.
Published: (1994) -
Direct asymmetric syntheses of chiral aldehydes and ketones via N-acyl chiral auxiliary derivatives including chiral Weinreb amide equivalents.
by: Davies, S, et al.
Published: (2013) -
ASYMMETRIC ALDOL AND ALKYLATION REACTIONS MEDIATED BY THE QUAT CHIRAL AUXILIARY (R)-(-)-5-METHYL-3,3-DIMETHYL-2-PYRROLIDINONE
by: Davies, S, et al.
Published: (1994)