Holz et al., 2017 - Google Patents
Manufacture of Citronellal by the Rhodium‐Catalyzed Homogeneous Hydrogenation of NeralHolz et al., 2017
- Document ID
- 17476520179444227419
- Author
- Holz J
- Doerfelt S
- Börner A
- Publication year
- Publication venue
- Advanced Synthesis & Catalysis
External Links
Snippet
The highly chemoselective hydrogenation of neral affording citronellal is described. The reaction has been conducted with homogeneous rhodium complexes. Among the set of ancillary diphosphane ligands tested, Xantphos was found to be superior. The relevant …
- WTEVQBCEXWBHNA-JXMROGBWSA-N citral A 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CC(C)=CCC\C(C)=C\C=O 0 title abstract description 108
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
- B01J31/1805—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing nitrogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
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Chakraborty et al. | Well-defined iron catalysts for the acceptorless reversible dehydrogenation-hydrogenation of alcohols and ketones | |
Li et al. | Hydrogenation of benzonitrile to benzylamine catalyzed by ruthenium hydride complexes with P− NH− NH− P tetradentate ligands: evidence for a hydridic− protonic outer sphere mechanism | |
Garbe et al. | Enantioselective hydrogenation of ketones using different metal complexes with a chiral PNP pincer ligand | |
Morimoto et al. | Evolution of carbonylation catalysis: no need for carbon monoxide | |
Ahlin et al. | Nickel (0)‐catalyzed enantioselective annulations of alkynes and arylenoates enabled by a chiral NHC ligand: efficient access to cyclopentenones | |
Pannetier et al. | Cyclometalated complexes of ruthenium, rhodium and iridium as catalysts for transfer hydrogenation of ketones and imines | |
Heller et al. | On the Enantioselective Hydrogenation of Isomeric Methyl 3‐Acetamidobutenoates with RhI Complexes | |
Funk et al. | Synthesis and Catalytic Activity of (3, 4-Diphenylcyclopentadienone) Iron Tricarbonyl Compounds in Transfer Hydrogenations and Dehydrogenations | |
Vander Mierde et al. | A Ruthenium‐Catalyzed Approach to the Friedländer Quinoline Synthesis | |
Salamanca et al. | [2, 2′-Bipyridin]-6 (1 H)-one, a Truly Cooperating Ligand in the Palladium-Mediated C–H Activation Step: Experimental Evidence in the Direct C-3 Arylation of Pyridine | |
Baldino et al. | Transfer Hydrogenation and Hydrogenation of Commercial‐Grade Aldehydes to Primary Alcohols Catalyzed by 2‐(Aminomethyl) pyridine and Pincer Benzo [h] quinoline Ruthenium Complexes | |
Kotha et al. | An efficient, stable and reusable Palladium nanocatalyst: Chemoselective reduction of aldehydes with molecular hydrogen in water | |
Borrego et al. | An efficient and practical method for the enantioselective synthesis of tertiary trifluoromethyl carbinols |