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Keyphrases
Enantioselectivity
100%
Gabosine
87%
Enantioselective Synthesis
65%
Alkaloids
58%
Securinega Alkaloids
51%
Ring-closing Metathesis
45%
Norsecurinine
43%
Vinyl Ether
43%
Cu(II)
39%
Vinylogous Mannich Reaction
36%
Overall Yield
34%
Platinum Complexes
34%
Pt(II) Complexes
34%
Palladium Catalysis
34%
Azaphenalene
29%
Divergent Approach
29%
Tert-butyl
29%
Cycloaddition
29%
1,3-dipolar Cycloaddition
29%
Total Synthesis
29%
Azobenzene
29%
Imide
24%
Stereoselectivity
22%
Glutarimides
21%
Allylic Alcohols
21%
Efficient Protocol
21%
Synthetic Approaches
21%
Synthetic Study
21%
Stereoselective Synthesis
21%
Ti(IV)
21%
Cu(I)
19%
Cisplatin
19%
A2780
19%
Anticancer Activity
19%
Cu(II) Complex
19%
Allyl
18%
Relative Configuration
18%
Cancer Cell Lines
17%
Allylation
17%
Cisplatin Resistance
17%
Mass Spectrometry
17%
Cyclohexanone
16%
Cytotoxicity
15%
Reactive Oxygen Species
14%
Ovarian Cancer Cells
14%
Platinum-resistant Ovarian Cancer
14%
Sulfonamides
14%
Bidentate Ligands
14%
Allosecurinine
14%
Configuration Assignment
14%
Chemistry
Enantioselective Synthesis
80%
Ring Closing Metathesis
65%
Enantiomer
58%
Palladium
58%
Imide
51%
Mannich Reaction
48%
Cisplatin
45%
Vinyl Ether
43%
Reactive Oxygen Species
36%
Allylation
36%
1,3-cycloaddition
29%
Stereoselective Synthesis
29%
Alkylation
29%
Cycloaddition
29%
Allylic Alcohol
29%
Azobenzene
29%
Cyclohexane
26%
IC50
26%
formation
23%
Enantioselectivity
21%
Cyclohexenone
21%
Absolute Configuration
21%
Bioactivity
19%
epoxidation
19%
Dimethyl Sulfoxide
17%
Mass Spectrometry
17%
Metabolite
14%
Diastereoselectivity
14%
Securinine
14%
Cell-Penetrating Peptide
14%
Metathesis Reaction
14%
Allylic Alkylation
14%
Enol
14%
2-Epi-5-Epi-Valiolone
14%
Desulfurization
14%
Ketones
14%
Enone
14%
Epimer
14%
Nitrone
14%
Paclitaxel
14%
Epoxide
14%
methylation
14%
Enzymatic Hydrolysis
14%
Natural Product
14%
Stereoisomer
14%
Stemona Alkaloid
14%
Secondary Metabolite
14%
Density Functional Theory
14%
Diastereoselective Synthesis
14%
Acetylation
14%