Is this you? As a journalist, you can create a free Muck Rack account to customize your profile, list your contact preferences, and upload a portfolio of your best work.
Claim your profile
Articles by Christoph Zippel
Diversity‐Oriented Synthesis of [2.2]Paracyclophane‐derived Fused Imidazo[1,2‐a]heterocycles by Groebke‐Blackburn‐Bienaymé Reaction: Accessing Cyclophanyl Imidazole Ligands Library
Abstract Diversified Groebke-Blackburn-Bienaymé Approach: Diversity-oriented synthesis of cyclophanyl-derived fused imidazo[1,2-a]heterocycles by one-pot Groebke-Blackburn-Bienaymé (GBB) three-component reaction employing formyl-cyclophane components in combination with various aliphatic and aromatic isocyanides and different heteroaromatic amidines is described. Additionally, a one-pot protocol for the GBB 3CR process by an in-situ generation of cyclophanyl isocyanide is demonstrated.
Skeletal Editing-Nitrogen Deletion of Secondary Amines by Anomeric Amide Reagents
Highlight Christoph Zippel, Institute of Organic Chemistry (IOC), Karlsruhe Institute of Technology (KIT), Fritz-Haber-Weg 6, 76131 Karlsruhe, Germany Search for more papers by this author Jasmin Seibert, Institute of Organic Chemistry (IOC), Karlsruhe Institute of Technology (KIT), Fritz-Haber-Weg 6, 76131 Karlsruhe, Germany Search for more papers by this author Prof.
A Highly Stable, Au/Ru Heterobimetallic Photoredox Catalyst with a [2.2]Paracyclophane Backbone
This article is Open Access Please wait while we load your content... Something went wrong. Try again?
Metal-supported and -assisted stereoselective cooperative photoredox catalysis
This article is Open Access Please wait while we load your content... Something went wrong. Try again?
Show More
loading
Actions
Is this you?
As a journalist, you can create a free Muck Rack account to customize your profile, list your contact preferences, and upload a portfolio of your best work.Get in touch with Christoph
Contact Christoph, search articles and posts on X, monitor coverage, and track replies from one place.
Learn more about Muck Rack