This search combines search strings from the content search (i.e. "Full Text", "Author", "Title", "Abstract", or "Keywords") with "Article Type" and "Publication Date Range" using the AND operator.
Beilstein J. Org. Chem. 2022, 18, 303–308, doi:10.3762/bjoc.18.34
Graphical Abstract
Scheme 1: Reaction conducted according to the Ellman protocol.
Figure 1: Asymmetric unit of 2a, with the atom-numbering scheme. The crystallographic reference system is als...
Figure 2: Substrate scope of the borylcopper-mediated homocoupling of oxindole-based N-tert-butanesulfinyl im...
Scheme 2: Proposed mechanism for the borylcopper-mediated homocoupling of ketimines 1.
Beilstein J. Org. Chem. 2014, 10, 1383–1389, doi:10.3762/bjoc.10.141
Figure 1: Biologically active agents containing a 3-substituted-3-aminooxindole core.
Figure 2: ORTEP [37] view of one of the two independent molecules of 4a present in the asymmetric unit, showing t...
Figure 3: Proposed explanation of the stereochemical outcome of the Ugi 3CR.
Scheme 1: Post-Ugi transformation on compound 10a.
Scheme 2: Post-Ugi cyclization on compound 15a.
Beilstein J. Org. Chem. 2013, 9, 147–154, doi:10.3762/bjoc.9.17
Figure 1: THBC-DKP-based natural and synthetically made compounds.
Figure 2: THBC-DKP-based peptidomimetic 1a.
Figure 3: Geometric parameters for mimics 1a,b.
Figure 4: Perspective view of the low-energy conformers of 1a,b. Hydrogen atoms are omitted for clarity.
Scheme 1: Synthesis of the THBC-DKP-based peptidomimetic 1a.