This search combines search strings from the content search (i.e. "Full Text", "Author", "Title", "Abstract", or "Keywords") with "Article Type" and "Publication Date Range" using the AND operator.
Beilstein J. Org. Chem. 2015, 11, 530–562, doi:10.3762/bjoc.11.60
Generic mechanism for the conjugate addition reaction.
Methods to activate unsaturated amide/lactam systems.
DCA of Grignard reagents to an L-ephedrine derived chiral α,β–unsaturated amide.
Chiral auxiliaries used in DCA reactions.
Comparison between auxiliary 5 and the Oppolzer auxiliary in a DCA reaction.
Use of Evans auxiliary in a DCA reaction.
Lewis acid complex of the Evans auxiliary .
DCA reactions of α,β-unsaturated amides utilizing (S,S)-(+)-pseudoephedrine and the OTBS-derivative...
Proposed model accounting for the diastereoselectivity observed in the 1,4-addition of Bn2NLi to α,...
An example of a tandem conjugate addition–α-alkylation reaction of an α,β-unsaturated amide utilizi...
Conjugate addition to an α,β-unsaturated bicyclic lactam leading to (+)-paroxetine and (+)-femoxeti...
Intramolecular conjugate addition reaction to α,β-unsaturated amide.
Conjugate addition to an α,β-unsaturated pyroglutamate derivative.
Cu(I)–NHC-catalyzed asymmetric silylation of α,β-unsaturated lactams and amides.
Asymmetric copper-catalyzed 1,4-borylation of an α,β-unsaturated amide.
Asymmetric cross-coupling 49 to phenyl chloride.
Rhodium-catalyzed asymmetric 1,4-arylation of an α,β-unsaturated lactam.
Rhodium-catalyzed asymmetric 1,4-arylation of an α,β-unsaturated amide.
Rhodium-catalyzed asymmetric 1,4-arylation of an α,β-unsaturated amide using a chiral bicyclic dien...
Synthesis of (R)-(−)-baclofen through a rhodium-catalyzed asymmetric 1,4-arylation of lactam 58.
Rhodium-catalyzed asymmetric 1,4-arylation of an α,β-unsaturated amide and lactam employing organo[...
Rhodium-catalyzed asymmetric 1,4-arylation of an α,β-unsaturated lactam employing benzofuran-2-ylzi...
Further chiral ligands that have been used in rhodium-catalyzed 1,4-additions of α,β-unsaturated am...
Palladium-catalyzed asymmetric 1,4-arylation of arylsiloxanes to a α,β-unsaturated lactam.
SmI2-mediated cyclization of α,β-unsaturated Weinreb amides.
Chiral Lewis acid complexes used in the Mukaiyama–Michael addition of α,β-unsaturated amides.
Mukaiyama–Michael addition of thioester silylketene acetal to α,β-unsaturated N-alkenoyloxazolidino...
Asymmetric 1,4-addition of aryl acetylides to α,β-unsaturated thioamides.
Asymmetric 1,4-addition of alkyl acetylides to α,β-unsaturated thioamides.
Asymmetric vinylogous conjugate additions of unsaturated butyrolactones to α,β-unsaturated thioamid...
Gd-catalyzed asymmetric 1,4-cyanation of α,β-unsaturated N-acylpyrroles .
Lewis acid-catalyzed asymmetric 1,4-cyanation of α,β-unsaturated N-acylpyrazole 107.
Lewis acid mediated 1,4-addition of dibenzyl malonate to α,β-unsaturated N-acylpyrroles.
Chiral Lewis acid mediated 1,4-radical addition to α,β-unsaturated N-acyloxazolidinone .
Aza-Michael addition of O-benzylhydroxylamine to an α,β-unsaturated N-acylpyrazole.
An example of the aza-Michael addition of secondary aryl amines to an α,β-unsaturated N-acyloxazoli...
Aza-Michael additions of anilines to a α,β-unsaturated N-alkenoyloxazolidinone catalyzed by palladi...
Aza-Michael additions of aniline to an α,β-unsaturated N-alkenoylbenzamide and N-alkenoylcarbamate ...
Difference between aza-Michael addition ran using the standard protocol versus the slow addition pr...
Aza-Michael additions of aryl amines salts to an α,β-unsaturated N-alkenoyloxazolidinone catalyzed ...
Aza-Michael addition of N-alkenoyloxazolidiniones catalyzed by samarium diiodide .
Asymmetric aza-Michael addition of p-anisidine to α,β-unsaturated N-alkenoyloxazolidinones catalyze...
Asymmetric aza-Michael addition of O-benzylhydroxylamine to N-alkenoyloxazolidinones catalyzed by i...
Asymmetric 1,4-addition of purine to an α,β-unsaturated N-alkenoylbenzamide catalyzed by (S,S)-(sal...
Asymmetric 1,4-addition of phosphites to α,β-unsaturated N-acylpyrroles.
Asymmetric 1,4-addition of phosphine oxides to α,β-unsaturated N-acylpyrroles.
Tandem Michael-aldol reaction catalyzed by a hydrogen-bonding organocatalyst.
Examples of the sulfa-Michael–aldol reaction employing α,β-unsaturated N-acylpyrazoles.
Example of the sulfa-Michael addition of α,β-unsaturated N-alkenoyloxazolidinones.
Structure of cinchona alkaloid-based squaramide catalyst.
Asymmetric intramolecular oxa-Michael addition of an α,β-unsaturated amide.
Formal synthesis atorvastatin.