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Web Date: June 30, 2015
Web Date: June 30, 2015
New Route To Rare Heterocycles
Organic Synthesis: Surprisingly stable dicarbonyls react to yield unusual ring-based products
Department: Science & Technology
News Channels: Organic SCENE
Keywords: heterocycles, organic synthesis, N-methyliminodiacetic acid (MIDA), amphoteric
News Channels: Organic SCENE
Keywords: heterocycles, organic synthesis, N-methyliminodiacetic acid (MIDA), amphoteric
Researchers have created a series of unexpectedly stable boryl-dicarbonyl compounds and have used them to synthesize heterocyclic molecules that were previously difficult or impossible to make.
According to conventional wisdom among chemists, because the boryl-dicarbonyls have multiple reactive groups in close proximity, they should break down quickly. In this new work, however, they are stable and can undergo double-condensation reactions that result in ring formation. The heterocyclic products of these reactions could be useful as . . .
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- Chemical & Engineering News
- ISSN 0009-2347
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