|
Volumn , Issue 16, 2011, Pages 2579-2589
|
Palladium-catalyzed ligand-directed oxidative functionalization of cyclopropanes
|
Author keywords
C H functionalization; cleavage; cyclopropane; homogeneous catalysis; palladium
|
Indexed keywords
BENZOQUINONES;
C-C ACTIVATIONS;
C-H FUNCTIONALIZATION;
CLEAVAGE;
CYCLOPROPANE;
CYCLOPROPANE RING;
FUNCTIONALIZATIONS;
HOMOGENEOUS CATALYSIS;
OXAZOLINES;
OXIDATIVE FUNCTIONALIZATION;
OXIME ETHERS;
PRODUCT DISTRIBUTIONS;
CATALYSIS;
ETHERS;
OXIDANTS;
REACTION KINETICS;
PROPANE;
1 (1 METHYLCYCLOPROPYL)ETHANONE O METHYLOXIME;
1 (3 ETHYLPYRIDIN 2 YL)PROPANE 1,2,3 TRIYL TRIACETATE;
1 (3 METHYLPYRIDIN 2 YL)PROPANE 1,2,3 TRIYL TRIACETATE;
1 CYCLOPROPYL 5 PHENYLPENTAN 2 ONE O METHYLOXIME;
1 CYCLOPROPYLHEXAN 1 ONE O METHYLOXIME;
2 (2 IODOCYCLOPROPYL) 3 ETHYLPYRIDINE;
2 (2 IODOCYCLOPROPYL) 3 METHOXYPYRIDINE;
2 (2 IODOCYCLOPROPYL) 3 METHYLPYRIDINE;
2 [2 (METHOXYIMINO) 5 PHENYLPENTYL]PROP 1 ENE 1,3 DIYL DIACETATE;
2 [2 (METHOXYIMINO) 5 PHENYLPENTYLIDENE]PROPANE 1,3 DIYL DIACETATE;
2 CYCLOPROPYL 3 ETHYLPYRIDINE;
2 CYCLOPROPYL 3 METHOXYPYRIDINE;
2 CYCLOPROPYL 3 METHYLPYRIDINE;
2 CYCLOPROPYL 4 METHYLPYRIDINE;
2 CYCLOPROPYL 6 METHYLPYRIDINE;
3 (4 TERT BUTYL 4,5 DIHYDROOXAZOL 2 YL)BUT 2 EN 1 YL ACETATE;
3 HYDROXY 4 (METHOXYIMINO) 3 METHYLPENTANE 1,2 DIYL DIACETATE;
4 (METHOXYIMINO) 2 METHYLPENT 2 EN 1 YL ACETATE;
4 (METHOXYIMINO)NON 2 EN 1 YL ACETATE;
4 TERT BUTYL 2 (1 METHYLCYCLOPROPYL) 4,5 DIHYDROOXAZOL 3 IUM;
4 TERT BUTYL 2 (1 METHYLCYCLOPROPYL) 4,5 DIHYDROOXAZOLE;
4 TERT BUTYL 2 CYCLOPROPYL 4,5 DIHYDROOXAZOL 3 IUM;
4 TERT BUTYL 2 CYCLOPROPYL 4,5 DIHYDROOXAZOLE;
5 (METHOXYIMINO) 8 PHENYLOCT 3 ENE 1,2 DIYL DIACETATE;
BENZOQUINONE;
CYCLOPROPANE DERIVATIVE;
LIGAND;
OXIDIZING AGENT;
PALLADIUM;
UNCLASSIFIED DRUG;
ACETOXYLATION;
ARTICLE;
CATALYSIS;
CATALYST;
CHEMICAL BOND;
CHEMICAL MODIFICATION;
CHEMICAL REACTION;
CHEMICAL STRUCTURE;
IODINATION;
OXIDATION;
PROTON NUCLEAR MAGNETIC RESONANCE;
PROTON TRANSPORT;
REACTION TIME;
RING OPENING;
ROOM TEMPERATURE;
TEMPERATURE DEPENDENCE;
|
EID: 80051545816
PISSN: 00397881
EISSN: 1437210X
Source Type: Journal
DOI: 10.1055/s-0030-1260087 Document Type: Article |
Times cited : (29)
|
References (38)
|