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Gold Catalysis: Evidence for the In‐situ Reduction of Gold(<scp>III</scp>) During the Cyclization of Allenyl Carbinols
European Journal of Organic Chemistry · 2006 · Vol. 2006(6) · pp. 1387–1389
A. Stephen K. Hashmi✉(Goethe University Frankfurt)M. Carmen Blanco(University of Stuttgart)Dirk Fischer(Goethe University Frankfurt)Jan W. Bats(Goethe University Frankfurt)
Abstract
Abstract Products of an oxidative coupling were obtained in the gold( III )‐catalyzed cycloisomerization of tertiary allenyl carbinols. The absence of reduced organic products and an increase of these coupling products with the amount of gold( III ) catalyst suggests that gold( III ) is reduced in situ, possibly to gold( I ) catalysts which were also shown to be active for these transformations. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006)
Catalytic Alkyne ReactionsOxidative Organic Chemistry ReactionsSynthetic Organic Chemistry MethodsCycloisomerizationChemistryCatalysisIn situOxidative coupling of methaneCoupling (piping)Medicinal chemistryOrganic chemistryCombinatorial chemistryMetallurgy
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References
Phosphine Gold(I) Bis-(trifluoromethanesulfonyl)imidate Complexes as New Highly Efficient and Air-Stable Catalysts for the Cycloisomerization of Enynes
Organic Letters · 2005 · 685 citations
The golden gate to catalysis
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