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Enantioselective synthesis of cyclic carbamimidates via a three-component reaction of imines, terminal alkynes, and p-toluenesulfonylisocyanate using a monophosphine gold(i) catalyst

✍ Scribed by Campbell, Matthew J.; Toste, F. Dean

Book ID
111650701
Publisher
The Royal Society of Chemistry
Year
2011
Tongue
English
Weight
249 KB
Volume
2
Category
Article
ISSN
2041-6520

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ChemInform Abstract: Enantioselective Sy
ChemInform Abstract: Enantioselective Synthesis of Cyclic Carbamimidates via a Three-Component Reaction of Imines, Terminal Alkynes, and p-Toluenesulfonylisocyanate Using a Monophosphine Gold(I) Catalyst.
✍ Matthew J. Campbell; F. Dean Toste πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons βš– 55 KB πŸ‘ 1 views

## Abstract In all cases, a mixture of five‐ and six‐membered rings is obtained favoring oxazole derivatives (ratio 1,6:1 up to β‰₯ 20:1).