Publication | Closed Access
Microwave-Enhanced Synthesis of N-Shifted Buflavine Analogues via a Suzuki−Ring-Closing Metathesis Protocol
68
Citations
10
References
2005
Year
Suzuki−ring-closing Metathesis ProtocolDiversity Oriented SynthesisAlkene MetathesisNatural SciencesDiversity-oriented SynthesisRing-closing Metathesis ReactionOrganic ChemistryMicrowave IrradiationChemistrySynthesis MethodMicrowave SynthesisSynthetic ChemistryMicrowave-enhanced SynthesisN-shifted Buflavine Analogues
[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.
| Year | Citations | |
|---|---|---|
Page 1
Page 1