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Abstract
A convenient microwave accelerated cross-coupling procedure between aryl chlorides with a range of boronic acids has been developed. An explanation for the low reactivity of highly fluorinated boronic acids in Suzuki coupling is provided.
Original language | English |
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Article number | 18 |
Number of pages | 4 |
Journal | Beilstein Journal of Organic Chemistry |
Volume | 3 |
DOIs | |
Publication status | Published - 30 May 2007 |
Keywords
- II RECEPTOR ANTAGONIST
- FREE HIYAMA REACTION
- EFFICIENT SYNTHESIS
- ARYLBORONIC ACIDS
- ORGANIC-SYNTHESIS
- ROOM-TEMPERATURE
- SODIUM-HYDROXIDE
- STILLE REACTION
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Dive into the research topics of 'A convenient catalyst system for microwave accelerated cross-coupling of a range of aryl boronic acids with aryl chlorides'. Together they form a unique fingerprint.Projects
- 1 Finished
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EPSRC EP/C014545/1: Activating organosilicon nucleophiles for catalytic C-C bond formation
Clarke, M. (PI)
1/10/05 → 30/09/08
Project: Standard