|
(3+2) cycloaddition |
1 |
|
[2, 3]-sigmatropic rearrangement |
1 |
|
[2,3]-sigmatropic rearrangement |
1 |
|
active methylene compound |
1 |
|
allylation |
1 |
|
allylic phenyl sulfides |
1 |
|
amines |
1 |
|
amino acid sequence |
1 |
|
aminoallyl |
1 |
|
aryl-x bond activation |
1 |
|
arylation |
1 |
|
asymmetric addition |
1 |
|
atom |
1 |
|
auto-tandem catalysis |
1 |
|
benzocyclobutenones |
1 |
|
c-c activation |
1 |
|
c-h activation |
1 |
|
carbonyl compounds β-ch bonds |
1 |
|
catalysis |
1 |
|
catalytic reaction |
1 |
|
cc bond formation |
1 |
|
ch functionalization |
1 |
|
cobalt catalysis |
1 |
|
conjugate addition |
1 |
|
cross-coupling |
1 |
|
cyanosilylation |
1 |
|
cyclization |
1 |
|
desymmetrization |
1 |
|
dienes |
1 |
|
enantioconvergent |
1 |
|
geometry |
1 |
|
homogeneous catalysis |
1 |
|
hydrazones |
1 |
|
ketone dehydrogenation |
1 |
|
ketones |
1 |
|
kinetic resolution |
1 |
|
metal carbene |
1 |
|
migratory group |
1 |
|
n-tosylhydrazone |
1 |
|
nitrogen heterocycles |
1 |
|
oxidation |
1 |
|
oxidative coupling |
1 |
|
palladium |
1 |
|
palladium-catalyzed redox cascade methods |
1 |
|
propargyl phenyl sulfides |
1 |
|
pyrrolidines |
1 |
|
quaternary stereocenter |
1 |
|
quaternary stereocenters |
1 |
|
redox-neutral catalysis |
1 |
|
sulfur ylide |
1 |
|
sulfur ylides |
1 |
|
synthetic methods |
1 |
|
vicinal stereocenters |
1 |
|
β-arylation of ketones |
1 |
|
β-naphthol |
1 |
