M
Martin N. Ackermann
Researcher at Heidelberg University
Publications - 25
Citations - 498
Martin N. Ackermann is an academic researcher from Heidelberg University. The author has contributed to research in topics: Catalysis & Allylic rearrangement. The author has an hindex of 10, co-authored 24 publications receiving 462 citations.
Papers
More filters
Journal ArticleDOI
On Homogeneous Gold/Palladium Catalytic Systems
A. Stephen K. Hashmi,Christian Lothschütz,René Döpp,Martin N. Ackermann,Janosc De Buck Becker,Matthias Rudolph,Christian Scholz,Frank Rominger +7 more
TL;DR: In this paper, the gold-and palladium-catalysed cross-coupling reactions were investigated on two substrates containing an aryl iodide and an allenoate ester.
Journal ArticleDOI
Gold catalysis: in situ EXAFS study of homogeneous oxidative esterification.
A. Stephen K. Hashmi,Christian Lothschütz,Martin N. Ackermann,Rene Doepp,Sankaran Anantharaman,Benjamin Marchetti,Helmut Bertagnolli,Frank Rominger +7 more
TL;DR: The in situ extended X-ray absorption fine structure study of the reactions indicated that the reaction mixtures contained only mononuclear gold species, the first proof for a homogeneous gold-catalysed oxidation reaction.
Journal ArticleDOI
Light‐Induced Mechanistic Divergence in Gold(I) Catalysis: Revisiting the Reactivity of Diazonium Salts
Svenja Taschinski,René Döpp,Martin N. Ackermann,Frank Rominger,Folkert de Vries,Maximilian F. S. J. Menger,Matthias Rudolph,A. Stephen K. Hashmi,A. Stephen K. Hashmi,Johannes E. M. N. Klein +9 more
TL;DR: In this paper, the same authors reported that the same vinyl AuI intermediate is capable of producing the observed products under photolytic and thermal conditions, without the need for an additional photo(redox) catalyst under aerobic conditions.
Journal ArticleDOI
[3,3]‐Sigmatropic Rearrangement Step in the Gold‐Catalyzed Cyclization of Allyl‐(ortho‐alkinylphenyl)methyl Ethers
Martin N. Ackermann,Janina Bucher,Melissa Rappold,Katharina Graf,Frank Rominger,A. Stephen K. Hashmi +5 more
TL;DR: The mechanistic studies show an allylic inversion, as supported by NMR data and an X-ray crystal structure analysis, as well as an intermolecular reaction, as determined by crossover experiments and clearly indicate product formation by a [3,3]sigmatropic rearrangement in the step forming the new C-C bond.
Journal ArticleDOI
Gold(I)‐Catalyzed Domino Reaction of Allyl 2‐en‐4‐ynyl Ethers to 1,3,6‐Trien‐4‐yl Ketones
TL;DR: In this paper, the reaction proceeds under mild conditions which are crucial as harsher conditions would not be tolerated due to the high degree of conjugation in the products, which is crucial for the reaction.