Are There Metal Oxides That Prefer a [2 + 2] Addition over a [3 + 2] Addition to Olefins? Theoretical Study of the Reaction Mechanism of LReO3 Addition (L = O-, Cl, Cp) to Ethylene1-Reference-Cited by-同舟云学术

Are There Metal Oxides That Prefer a [2 + 2] Addition over a [3 + 2] Addition to Olefins? Theoretical Study of the Reaction Mechanism of LReO3 Addition (L = O-, Cl, Cp) to Ethylene1

Published:1999-02-24 Issue:10 Volume:121 Page:2021-2031
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Deubel Dirk V.¹,Frenking Gernot¹

Affiliation:

1. Contribution from Fachbereich Chemie, Philipps-Universität Marburg, Hans-Meerwein-Strasse, D-35032 Marburg, Germany

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja9829362

Reference38 articles.

1. N-Heterocyclic Carbene, Silylene, and Germylene Complexes of MCl (M = Cu, Ag, Au). A Theoretical Study1

2. Temperatureffekte bei der asymmetrischen Dihydroxylierung: Hinweise auf einen schrittweisen Mechanismus

3. The origin of high enantioselectivity in the dihydroxylation of olefins using osmium tetraoxide and cinchona alkaloid catalysts

4. Theoretische Untersuchungen schließen eine [2 + 2]-Addition als einleitenden Schritt der Osmiumtetroxid-katalysierten Dihydroxylierung von Alkenen aus

5. Theory Does Not Support an Osmaoxetane Intermediate in the Osmium-Catalyzed Dihydroxylation of Olefins

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