Keyphrases
2H-chromene
5%
Alkenes
30%
Alkenyl
20%
Alkyl
5%
Alkynes
40%
Allenes
20%
Allyl
20%
Aryl
5%
Asymmetric Catalysis
30%
Asymmetric Hydrophosphination
12%
Asymmetric Synthesis
7%
Atom Economy
13%
Axially chiral
20%
Axially chiral Styrenes
10%
Bidentate
6%
Catalytic System
10%
Chiral Bisphosphine Ligand
10%
Chiral Molecules
8%
Chiral Phosphines
17%
Chiral Phosphorus
16%
Cholesterol
5%
Co-catalytic
10%
Copper-catalyzed
23%
Cyclopropane Ring
6%
Cyclopropenes
20%
DFT Calculations
10%
Diamine
20%
Diastereomeric Excess
6%
Diastereoselective
20%
Diastereoselectivity
6%
Disubstituted
6%
Efficient Construction
5%
Enantioselectivity
93%
Functional Groups
5%
Good Yield
6%
High Enantioselectivity
6%
Hydroamination
20%
Hydrophosphinylation
100%
Isoquinoline
20%
Late-stage Functionalization
5%
Mechanistic Studies
6%
Methylene
20%
Modular Methodology
10%
New Platform
10%
Organic Synthesis
10%
P,N-ligands
6%
Palladium Catalysis
40%
Pd-catalyzed
11%
Percentage Yield
16%
Phosphine
12%
Phosphine Ligands
30%
Phosphine Oxide
30%
Phosphorus-rich
16%
Propylene
26%
Rapid Construction
5%
Reaction Pathway
10%
Regioselectivity
20%
Ring Opening
6%
Ring Strain
6%
Stereocenters
6%
Transition-metal-catalyzed
12%
Vicinal
6%
Chemistry
2H-Chromene
5%
Alkene
30%
Alkyne
40%
Allene
20%
Asymmetric Catalysis
29%
Asymmetric Synthesis
6%
Carbene
20%
Cyclopropane
30%
Cyclopropane Ring
10%
Cyclopropene
20%
Density Functional Theory
10%
Diastereomer
10%
Diastereoselectivity
10%
Enantioselectivity
29%
Hydroamination
20%
Isoquinoline
20%
Mechanistic Study
5%
Palladium
40%
Phosphine Oxide
30%
Phosphorus
20%
Ring Opening Reaction
5%
Styrene
10%
Transition Metal
12%