Microwave-Enhanced Synthesis of N-Shifted Buflavine Analogues via a Suzuki−Ring-Closing Metathesis Protocol
Organic Letters2005Vol. 7(13), pp. 2723–2726
Citations Over TimeTop 10% of 2005 papers
Abstract
[reaction: see text] A novel, microwave-enhanced six-step synthesis was devised for the synthesis of N-shifted buflavine analogues. Microwave-enhanced Suzuki-Miyaura cross-coupling and ring-closing metathesis reactions were used as the key steps. Microwave irradiation was found to enhance the ring-closing metathesis reaction to generate the otherwise difficultly obtainable medium-sized ring system of the target molecules.
Related Papers
- → Microwave‐Assisted Olefin Metathesis(2007)105 cited
- → The Application of Olefin Metathesis to the Synthesis of Biologically Active Macrocyclic Agents(2005)32 cited
- → Reversible Backbone Protection Enables Combinatorial Solid-Phase Ring-Closing Metathesis Reaction (RCM) in Peptides(2001)53 cited
- → Synthesis of Amphidinolide X(2009)
- → Ring-Closing Metathesis Approach to Quinolizinium Salts(2009)