Selective oxidation of glycerol by highly active bimetallic catalysts at ambient temperature under base-free conditions.
about
Propylene from renewable resources: catalytic conversion of glycerol into propylene.A tris(triazolate) ligand for a highly active and magnetically recoverable palladium catalyst of selective alcohol oxidation using air at atmospheric pressure.Tuning the composition of AuPt bimetallic nanoparticles for antibacterial applicationIn situ spectroscopic investigation of oxidative dehydrogenation and disproportionation of benzyl alcohol.Gold-nanoparticle-based catalysts for the oxidative esterification of 1,4-butanediol into dimethyl succinate.Catalytic oxidation of cinnamyl alcohol using Au-Ag nanotubes investigated by surface-enhanced Raman spectroscopy.The Role of Mg(OH)2 in the So-Called "Base-Free" Oxidation of Glycerol with AuPd Catalysts.Selective Hydrogenolysis of Glycerol to 1,3-Propanediol: Manipulating the Frustrated Lewis Pairs by Introducing Gold to Pt/WOx.Selective glycerol oxidation by electrocatalytic dehydrogenation.Efficient Generation of Lactic Acid from Glycerol over a Ru-Zn-CuI /Hydroxyapatite Catalyst.AuPt Alloy on TiO2: A Selective and Durable Catalyst for L-Sorbose Oxidation to 2-Keto-Gulonic Acid.Oxidation of Aliphatic Alcohols by Using Precious Metals Supported on Hydrotalcite under Solvent- and Base-Free Conditions.Selective oxidation of n-butanol using gold-palladium supported nanoparticles under base-free conditions.Multifunctional Heterogeneous Catalysts for the Selective Conversion of Glycerol into Methyl LactateTuning the Composition of AuPt Bimetallic Nanoparticles for Antibacterial ApplicationZeolite-supported bimetallic catalyst: controlling selectivity of rhodium complexes by nearby iridium complexes
P2860
Q30766893-00DB5571-8B77-4F7C-85FF-997B0CCA7D67Q33464354-A1E8BBDE-F564-4A03-AC15-392B9EE839E7Q35061102-1F51A60D-B9B3-4E7A-A6E0-0100816A59BCQ43416892-E8F9A2E6-A5FA-4D66-8566-047478DD5B70Q46593198-C626522F-8667-4FC3-B70A-40B8ED6456BDQ46740153-7313FB15-3F3F-4379-AAFD-B333A35D2875Q48368087-36B6476D-B3C6-462B-A164-CB71FB00FE49Q50272889-B677C5DB-B494-40FB-84A3-C376DAA42D8FQ50458924-4EB9D209-FC3C-4AB8-8210-235F29BC9D08Q50681887-7D3DD9C9-153B-4EB8-A570-791AC0D3B679Q51627804-DC3ACBBE-1BEE-4C1E-9EEB-09291A0B140CQ51784397-30646275-EEF9-45FB-8346-DBA637773013Q53244412-9C05A503-0A83-4BE2-88D7-134C2F146912Q57134894-57893710-4070-4FBF-9EAA-69F271420CBCQ57238708-3C87C6CA-BADC-4009-A421-ADAA72D3FDB5Q58019470-5021D27A-A62A-4025-80CD-0DDCFFD55830
P2860
Selective oxidation of glycerol by highly active bimetallic catalysts at ambient temperature under base-free conditions.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Selective oxidation of glycero ...... re under base-free conditions.
@ast
Selective oxidation of glycero ...... re under base-free conditions.
@en
type
label
Selective oxidation of glycero ...... re under base-free conditions.
@ast
Selective oxidation of glycero ...... re under base-free conditions.
@en
prefLabel
Selective oxidation of glycero ...... re under base-free conditions.
@ast
Selective oxidation of glycero ...... re under base-free conditions.
@en
P2093
P2860
P50
P356
P1476
Selective oxidation of glycero ...... ure under base-free conditions
@en
P2093
Andrew A Herzing
Ceri Hammond
Christopher J Kiely
David W Knight
Gemma L Brett
Graham J Hutchings
Peter J Miedziak
P2860
P304
10136-10139
P356
10.1002/ANIE.201101772
P407
P50
P577
2011-08-24T00:00:00Z