Keyphrases
1,2-cis
9%
1,3-Cyclohexanedione
20%
1,3-Diones
8%
1,3-dipolar Cycloaddition
16%
2,3-Sigmatropic Rearrangement
11%
2-Iodobenzamides
19%
2-substituted
9%
Acetal
16%
Alcohol
10%
Alcohol Oxidation
11%
Aldehydes
10%
Alkaloids
13%
Alkyl
19%
Alkylation
11%
Alkynes
11%
Allyl
13%
Amides
8%
Amination
8%
Amines
16%
Aryl
16%
Asymmetric Synthesis
23%
Benzene
13%
Biological Evaluation
9%
C-H Amination
19%
C-H Insertion
18%
C-H Insertion Reaction
37%
Carbonyl Ylide
29%
Carboxylate
36%
Catalytic Asymmetric Synthesis
12%
Cephalotaxine
9%
Chemoselective
15%
CIS2
10%
Co-oxidant
16%
Collidine
9%
Conjugate Addition
9%
Cycloaddition
8%
Diastereoselective
18%
Diastereoselectivity
9%
Diazo
39%
Diazoester
9%
Diazoketones
14%
Diphenyl Phosphate
9%
Dirhodium Complex
100%
Discorhabdin
10%
Disubstituted
10%
Double Bond
8%
Efficient Synthesis
22%
Enantioselectivity
52%
Ether
10%
Excellent Yields
23%
Furan
11%
Good Yield
13%
Hypervalent Iodine Oxidation
34%
Hypervalent Iodine Reagents
19%
Indole
18%
Insertion Reaction
12%
Intramolecular C-H Insertion
24%
Iodocyclization
20%
Keto Group
8%
Ketoesters
14%
Lactones
20%
Methanol
14%
Methyl
30%
Natural Products
11%
Opsin
8%
Optically Active
18%
Oxidative Cleavage
14%
Oxone
34%
Oxonium Ylide
23%
Pachastrissamine
9%
Percentage Yield
11%
Phenol Derivatives
14%
Phenol Oxidation
10%
Phenyl
11%
Phthaloyl Dichloride
17%
Polymer Support
13%
Quinones
23%
Radical Cyclization
8%
Radical Initiator
8%
Radical Reactions
9%
Regioselective Alkylation
10%
Regioselectivity
13%
Retinal Chromophore
8%
Rh(II)-catalyzed
17%
Rhodium(II)
19%
Ring-opening Cyclizations
33%
Room Temperature
22%
S-acetal
9%
Soluble Radical
8%
Spirocyclopropane
42%
Stereocontrolled
15%
Stereoselective Synthesis
29%
Stereoselectivity
43%
Styrene
9%
Tert
50%
Tetrahydrofuran
17%
Tetrakis
34%
Total Synthesis
23%
Trifluoroacetate
13%
Water-soluble
11%
Chemistry
1,3-cycloaddition
16%
2,2,2-trifluoroethanol
9%
2,3-dihydrobenzofuran
8%
3-Oxohexanoate
6%
Acetal
28%
Acetonitrile
9%
Acetyl
6%
Addition Reaction
6%
Alkene
15%
Alkyl Group
6%
Alkylation
17%
Alkyne
15%
Ambient Reaction Temperature
28%
amination
26%
Antitumor
6%
Asymmetric Synthesis
22%
Azide
9%
Baeyer-Villiger Oxidation
6%
Benzene
12%
Benzoquinone
6%
Boiling
6%
Carbonyl Compound
9%
Carbonyl Ylide
29%
Carboxamide
9%
Carboxylic Acid
46%
Catalysis
7%
Cephalotaxine
9%
Chelation
8%
Chemoselectivity
27%
Chromophore
12%
Cobalt
6%
Copolymerization
6%
Cycloaddition
18%
Cycloalkane
6%
cyclohexane-1,3-dione
20%
Cyclohexanedione
7%
Cyclopentane
6%
Cyclopentanone
6%
Diastereoselectivity
10%
Dichloromethane
11%
Diol
6%
Double Bond
9%
Enantioselectivity
15%
Ethyl
11%
formation
55%
Furan
14%
Hetero Diels-Alder Cycloaddition
6%
Heterocyclic Compound
10%
Hydrogen
7%
Hypervalence
50%
Immobilized Catalyst
6%
Immunomodulator
6%
Immunosuppressive Agent
6%
Indole
22%
Insertion Reaction
48%
Intramolecular Heck Reaction
6%
Iodoarene
8%
Ketoester
11%
Ketone
8%
Ketones
20%
Lactam
6%
Lactone
25%
Leucinate
28%
Lithium
6%
Methanol
14%
Monomer
6%
Myriocin
9%
Natural Product
17%
NMR Spectroscopy
9%
Nucleophile
15%
Octane
9%
oxidation of phenols
8%
Oxidative Elimination Reaction
14%
Oxonium Ylide
23%
Palladium
7%
Phenol
16%
Primary Alcohols
7%
Primary Amine
6%
Protecting Groups
8%
Quinone
28%
Radical Cyclization
8%
Radical Reaction
9%
Retinoic Acid
8%
Rhodium
22%
Ring Expansion
6%
Ring Opening Reaction
35%
Silyl Enol Ether
7%
Solid-State NMR
9%
Sphingosine
6%
Stereoselective Synthesis
27%
Stereoselectivity
14%
Styrene
9%
Sulfenylation
6%
Sulfonium
11%
Table Salt
8%
Tetrahydrofuran
19%
Thioester
6%
Trifluoroacetate
14%
Water Soluble
10%
Ylide
10%