Keyphrases
Dimethyl
100%
Diazomalonates
93%
Carbonyl Ylide
58%
Dihydrofuran
54%
Enaminones
41%
Carbonyl
37%
Carbenoids
35%
Diazocarbonyl Compounds
34%
Benzoxazine
30%
Oxazine
30%
Diazo Compounds
30%
One-pot Synthesis
27%
Ylide Reaction
27%
Naphthoxazine
27%
Enones
27%
Cu(OAc)2
26%
Conjugated Carbonyl Groups
23%
Polybenzoxazine
23%
Furyl
22%
Electrocyclic Ring Closure
20%
Reaction Pathway
20%
Diazo
19%
Propylene
18%
Ring-opening Copolymerization (ROCOP)
18%
Catalyzed Reaction
18%
Metal Carbenoids
18%
Copper(II)-catalyzed
17%
Esters
16%
Thiophenyl
15%
Ethyl Diazoacetate
14%
Dicarbonyl Compounds
13%
Graft Copolymer
13%
Triazinane
13%
Benzoxazine Monomer
13%
Pyrrole-based
13%
Non-axisymmetric
13%
Polyvinyl Alcohol
13%
Non-peripherally
13%
DFT Calculations
13%
Triazole
13%
Diastereoselective
13%
Formaldehyde
13%
Reaction Synthesis
13%
Click Chemistry
13%
Benzylidene
13%
Pyrrole
13%
ε-Caprolactone (ε-CL)
13%
Metallophthalocyanine
13%
Exchange Reaction
13%
Lactones
13%
Chemistry
Carbonyl Ylide
58%
Dihydrofuran
54%
Enaminone
41%
Diazo Compound
32%
formation
32%
Oxazine
27%
Enone
27%
Furan
23%
Cyclization Reaction
20%
Ethyl
18%
Chemoselectivity
18%
Cyclopropane
18%
Thiophene
18%
Product Distribution
17%
Mannich Reaction
16%
Metallophthalocyanine
13%
One Pot Reaction
13%
Naphthalenone
13%
Benzoxazine
13%
Synthesis Reaction
13%
Diester
13%
Ketones
13%
Pyrrole
13%
stability
13%
Triazinane
13%
Fourier Transform Infrared Spectroscopy
13%
Lactone
13%
Density Functional Theory
13%
Aldehyde
13%
Donor
13%
Carbene
12%
Ketone
11%
Heterocyclic Compound
10%
Primary Amine
9%
Carbonyl Compound
9%
2,3-dihydrofuran
9%
Diastereoselectivity
9%
Diastereomer
9%
Acetylacetonate
8%
Catalyst Activity
8%
Polyene
6%
NMR Spectroscopy
6%
Cyclopropene
6%
Carbonyl Reaction
6%
Ring Opening Polymerisation
6%
Gas Chromatography Mass Spectrometry (GCMS)
6%
Fourier Transform Infrared Spectroscopy
6%
Double Bond
6%
Butadiene
6%
Differential Scanning Calorimetry
6%
