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Beilstein J. Org. Chem. 2015, 11, 2254–2260, doi:10.3762/bjoc.11.245
Graphical Abstract
Scheme 1: The Au(I)-catalyzed skeletal rearrangement of the [2 + 2] cycloaddition of 1,6-enynes that involves...
Scheme 2: The catalytic activity of IPrAuCl + NaBArF4 in the carbene-transfer reaction to styrene or methanol....
Scheme 3: The gold-promoted decarbenation reaction described by Echavarren and co-workers.
Scheme 4: (a) General representation of the metal-catalyzed carbene-transfer reaction (olefin cyclopropanatio...
Figure 1: Plot of evolved nitrogen with time for the reactions of EDA with styrene or methanol.
Figure 2: Top: Plots of evolved nitrogen with time for the reactions of EDA with styrene (left) or methanol (...
Scheme 5: The outer- and inner-sphere routes for this transformation.
Figure 3: The experimental device for the measurement of N2 evolution.
Beilstein J. Org. Chem. 2011, 7, 653–657, doi:10.3762/bjoc.7.77
Scheme 1: (a) The Buchner reaction of benzene and ethyl diazoacetate and (b) the Rh-catalyzed version. (c) Bo...
Scheme 2: The Buchner reaction applied to naphthalene. (a) Teyssié's system. (b) Müller's system.
Scheme 3: The gold-catalyzed reaction of benzene and EDA.
Scheme 4: The functionalization of naphthalene with ethyl diazoacetate catalyzed by the complexes (a) 1a and ...
Scheme 5: The functionalization of naphthalene with ethyl 2-diazopropionate catalyzed by complexes 1a and 1b.