Generation and Oligomerization of N-Ferrocenyl Ketenimines via Open-Shell Intermediates
Author:
Affiliation:
1. Institute of Inorganic Chemistry and Analytical Chemistry, Johannes Gutenberg-University, Duesbergweg 10-14, D-55128 Mainz, Germany
Funder
European Cooperation in Science and Technology
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Link
http://pubs.acs.org/doi/pdf/10.1021/acs.organomet.6b00619
Reference77 articles.
1. Main Chain Ferrocenyl Amides from 1‐Aminoferrocene‐1′‐carboxylic Acid
2. Anion‐Induced Motion in a Ferrocene Diamide
3. Molecular Multi‐Wavelength Optical Anion Sensors
4. Oligonuclear Ferrocene Amides: Mixed‐Valent Peptides and Potential Redox‐Switchable Foldamers
5. Redox-responsive organometallic foldamers from ferrocene amino acid: Solid-phase synthesis, secondary structure and mixed-valence properties
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1. Unexpected C–C Bond Formation with a Ferrocenyl Fischer Carbene Complex;Zeitschrift für anorganische und allgemeine Chemie;2020-05-07
2. A Ferrocenyl Amino Substituted Stannylene as an Intramolecular Fe→Sn Lewis Adduct;Zeitschrift für anorganische und allgemeine Chemie;2018-08-30
3. Redox‐Controlled Stabilization of an Open‐Shell Intermediate in a Bioinspired Enzyme Model;European Journal of Inorganic Chemistry;2018-07-10
4. N-Cobaltocenium Amide as Reactive Nucleophilic Reagent for Donor–Acceptor Bimetallocenes;Organometallics;2017-12-05
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