A
Armin de Meijere
Researcher at University of Göttingen
Publications - 846
Citations - 23062
Armin de Meijere is an academic researcher from University of Göttingen. The author has contributed to research in topics: Organic synthesis & Cycloaddition. The author has an hindex of 56, co-authored 845 publications receiving 22211 citations. Previous affiliations of Armin de Meijere include University of Hamburg & Ivoclar Vivadent.
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Metal-catalyzed cross-coupling reactions
TL;DR: In this paper, the authors present an approach to the formation of C-X (X = N, O, S) bonds in metal-catalyzed cross-coupling reactions.
Journal ArticleDOI
Fine Feathers Make Fine Birds: The Heck Reaction in Modern Garb†
Armin de Meijere,Frank E. Meyer +1 more
TL;DR: The Heck reaction has been a topic of fluctuating interest; however, in the last six years activity in this area has flourished as discussed by the authors, leading to impressive sequences consisting of even different reaction types that occur not only in a consecutive mode, but also in a single operation.
Journal ArticleDOI
Bonding Properties of Cyclopropane and Their Chemical Consequences
TL;DR: The cyclopropane ring more closely resembles the CC double bond than the cyclobutane ring: it is a small ring with "double bond character" as mentioned in this paper, and while distinct differences in reactivity do exist, there are no fundamental differences in behavior.
Journal ArticleDOI
Isocyanides in the Synthesis of Nitrogen Heterocycles
TL;DR: Methods starting from isocyanides often have distinct advantages over alternative approaches to the same heterocycles because of their enhanced convergence, the great simplicity of most of the operations with them, and the great variety of isOCyanides readily available for use.
Journal ArticleDOI
A rational chemical synthesis of C60.
Lawrence T. Scott,Margaret M. Boorum,Brandon McMahon,Stefan Hagen,James Mack,Jarred T. Blank,Hermann A. Wegner,Hermann A. Wegner,Armin de Meijere +8 more
TL;DR: The methods developed for the target-specific synthesis of fullerenes, applied here to a synthesis of C60, should make possible the directed laboratory preparation of other fullerene as well, including those not accessible by graphite vaporization.