Journal
HETEROCYCLES
Volume 77, Issue 1, Pages 193-199Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.3987/COM-08-S(F)24
Keywords
Rhodium; Reaction in Water; Propargylic Oxirane; Addition; Diastereoselective
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Funding
- Japan Society for the Promotion of Science (JSPS)
- Takeda Science Foundation
- Astellas Foundation for Research on Medicinal Resources
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A diastereoselective coupling of propargylic oxiranes with arylboronic acids in aqueous condition is described. 4-Aryl-substituted 2,3-allenols having syn-geometries were selectively synthesized by the rhodium-catalyzed reactions in water.
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