TY - JOUR
T1 - Mehrfachbindungen zwischen Hauptgruppenelementen und übergangsmetallen, CVIII. Stöchiometrische und katalytische Oxidation elektronenarmer Olefine mit Osmiumtetraoxid
T2 - Eine neue Oxidationsmethode für Fluorolefine
AU - Herrmann, Wolfgang A.
AU - Eder, Stefan J.
PY - 1993/1
Y1 - 1993/1
N2 - Multiple Bonds between Atoms of Main Group Elements and Transition Metals, CVIII. — Stoichiometric and Catalytic Oxidation of Electron‐poor Olefins with Osmium Tetraoxide: A Novel Oxidation Method for Fluoroolefins In contrast to current opinion, osmium tetraoxide reacts even with very electron‐poor olefins. For example, both partially and fully fluorinated osmate(VI) esters 2 are thus formed from fluoroolefins 1 by cycloaddition. Hydrolysis of the osmate(VI) esters leads to the corresponding 1,2‐diols 3 and, eventually, consecutive fluoroorganic products by HF elimination. A catalytic version of this route opens a new, general, and efficient entry to oxidation products in fluoroolefin chemistry. Tetrahalide ethylene derivatives of formula py2O2Os(OCX2CX2O) (X = Cl, F) split off oxalyl halide upon thermal treatment with the complexes py2O2OsX2 thus being formed in good yields.
AB - Multiple Bonds between Atoms of Main Group Elements and Transition Metals, CVIII. — Stoichiometric and Catalytic Oxidation of Electron‐poor Olefins with Osmium Tetraoxide: A Novel Oxidation Method for Fluoroolefins In contrast to current opinion, osmium tetraoxide reacts even with very electron‐poor olefins. For example, both partially and fully fluorinated osmate(VI) esters 2 are thus formed from fluoroolefins 1 by cycloaddition. Hydrolysis of the osmate(VI) esters leads to the corresponding 1,2‐diols 3 and, eventually, consecutive fluoroorganic products by HF elimination. A catalytic version of this route opens a new, general, and efficient entry to oxidation products in fluoroolefin chemistry. Tetrahalide ethylene derivatives of formula py2O2Os(OCX2CX2O) (X = Cl, F) split off oxalyl halide upon thermal treatment with the complexes py2O2OsX2 thus being formed in good yields.
KW - Fluroroolefins
KW - Osmium tetraoxide, oxidation with
KW - cis‐Hydroxylation, catalytic
UR - http://www.scopus.com/inward/record.url?scp=84985653137&partnerID=8YFLogxK
U2 - 10.1002/cber.19931260106
DO - 10.1002/cber.19931260106
M3 - Artikel
AN - SCOPUS:84985653137
SN - 0009-2940
VL - 126
SP - 31
EP - 37
JO - Chemische Berichte
JF - Chemische Berichte
IS - 1
ER -