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Beilstein J. Org. Chem. 2016, 12, 1447–1452, doi:10.3762/bjoc.12.140
Graphical Abstract
Scheme 1: Scope of the reaction with other electrophiles. The [3 + 2] cycloaddition reaction of 0.5 M 1a (10 ...
Figure 1: Proposed catalytic cycle.
Beilstein J. Org. Chem. 2015, 11, 2007–2011, doi:10.3762/bjoc.11.217
Scheme 1: Standard reaction conditions.
Scheme 2: Formation of aliphatic chiral β-hydroxy nitrile 2g and its subsequent conversion into 4g.
Beilstein J. Org. Chem. 2011, 7, 735–739, doi:10.3762/bjoc.7.83
Figure 1: Schematic diagram of the continuous flow reactor (left) and the column top (right).
Scheme 1: Hydrogenation of ethyl cinnamate.
Scheme 2: Hydrogenation of trans-stilbene and trans-chalcone.
Scheme 3: Hydrogenation of nitrobenzene and deprotection of the Cbz group.
Scheme 4: Hydrogenation in water.