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Carbene‐Catalyzed Enantioselective Decarboxylative Annulations to Access Dihydrobenzoxazinones and Quinolones

Carbene‐Catalyzed Enantioselective Decarboxylative Annulations to Access Dihydrobenzoxazinones and Quinolones

Methodology

Lee, A.; Zhu, J. L.; Feoktistova, T.; Brueckner, A. C.; Cheong, P. H.-Y.; Scheidt, K. A.* Angew. Chem. Int. Ed. 2019, 58, 5941-5945. Featured in: List, B.; Schwengers, S. Synfacts 2019, 15 (08), 0929.
Reductive Annulations of Arylidene Malonates With Unsaturated Electrophiles Using Photoredox/Lewis Acid Cooperative Catalysis

Reductive Annulations of Arylidene Malonates With Unsaturated Electrophiles Using Photoredox/Lewis Acid Cooperative Catalysis

Methodology

Betori, R. C.; McDonald, B. R.; Scheidt, K. A.* Chem. Sci. 2019, 10, 3353-3359.
NHC-Catalyzed Formal [2+2] Annulations of Allenoates for the Synthesis of Substituted Oxetanes

NHC-Catalyzed Formal [2+2] Annulations of Allenoates for the Synthesis of Substituted Oxetanes

Methodology

Lopez, S. S.; Jaworski, A. A.; Scheidt, K. A.* J. Org. Chem. 2018, 83, 14637-14645. Featured in: Snieckus, V.; da Frota, L. C. R. M. Synfacts 2019, 15 (02), 0124.
A Cooperative Hydrogen Bond Donor/Brønsted Acid System for the Enantioselective Synthesis of Tetrahydropyrans

A Cooperative Hydrogen Bond Donor/Brønsted Acid System for the Enantioselective Synthesis of Tetrahydropyrans

Methodology

Maskeri, M. A.; O’Connor, M. J.; Jaworski, A. A.; Bay, A. V.; Scheidt, K. A.* Angew. Chem. Int. Ed. 2018, 57, 17225-17229.
Intermolecular Reductive Couplings of Arylidene Malonates via Lewis Acid/Photoredox Cooperative Catalysis

Intermolecular Reductive Couplings of Arylidene Malonates via Lewis Acid/Photoredox Cooperative Catalysis

Methodology

McDonald, B. R.; Scheidt, K. A.* Org. Lett. 2018, 20, 6877-6881.
Enantioselective Synthesis of α-Amidoboronates Catalyzed by Planar-Chiral NHC-Cu(I) Complexes

Enantioselective Synthesis of α-Amidoboronates Catalyzed by Planar-Chiral NHC-Cu(I) Complexes

Methodology

Schwamb, C. B.; Fitzpatrick, K. P.; Brueckner, A. C.; Richardson, H. C.; Cheong, P. H.-Y.; Scheidt, K. A.* J. Am. Chem. Soc. 2018, 140 (34), 10644-10648.
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