Keyphrases
Olefins
100%
Diols
100%
Cyclopentadienone
100%
Rhenium Complexes
100%
Deoxydehydration
100%
Bio-based Polyols
100%
Rhenium
27%
Vicinal Diol
27%
Hydroxyl Group
18%
Polyol
18%
Butadiene
18%
Catalytic Activity
9%
Small Changes
9%
Reaction Mechanism
9%
Reaction Conditions
9%
DFT Study
9%
Dehydration Reaction
9%
Glycerol
9%
Cellulose
9%
Starch
9%
Further Development
9%
Deoxygenation
9%
High Oxygen Content
9%
Chemical Industry
9%
Excellent Yields
9%
Kinetic Study
9%
Major Components
9%
Pyridine
9%
Catalyst Stability
9%
Allylic Alcohols
9%
PPh3
9%
Structure-activity Relationship
9%
Tert
9%
Lignocellulosic Biomass
9%
Lignin
9%
Spectroscopic Characterization
9%
Renewable Sources
9%
Aromatic Compounds
9%
Sustainable Production
9%
Chemical Building Blocks
9%
High Turnover number
9%
Erythritol
9%
Xylitol
9%
Sorbitol
9%
Biomass Pretreatment
9%
High-valent
9%
Polyenes
9%
Dehydroxylation
9%
Sugar Compounds
9%
Octanol
9%
Triphenylphosphine
9%
Tert-butyl Group
9%
Catalytic Effect
9%
Polyol Compounds
9%
Ligand Substitution
9%
Substituted Cyclopentadienyl Ligand
9%
Cyclopentadienyl Ligands
9%
Reductive Deoxygenation
9%
Aliphatic-aromatic
9%
Polymeric Complex
9%
Percentage Yield
9%
Improved Catalysts
9%
Deoxygenation Reaction
9%
Dioxo
9%
Chemistry
Alkene
100%
Rhenium
100%
Polyol
100%
Cyclopentadienyl
100%
Diol
100%
stability
27%
formation
27%
Hydroxyl Group
18%
Butadiene
18%
Density Functional Theory
9%
Deoxygenation
9%
Turnover Number
9%
Triphenylphosphine
9%
Cellulose
9%
Polyene
9%
Allyl Alcohol
9%
Structure-Activity Relationship
9%
Chemical Industry
9%
Aromatic Compound
9%
3-Octanol
9%
Tert-Butyl Group
9%
Reductive Deoxygenation
9%
Dehydroxylation
9%
Catalyst Activity
9%
catalyst stability
9%
Erythritol
9%
Xylitol
9%
Glycerol
9%
Chemical Engineering
Olefin
100%
Rhenium
100%
Polyol
100%
Butadiene
25%
Aromatic Compound
12%