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6 in total

1. N-Substituted tertiary and O-substituted quaternary carbon stereogenic centers by site-, diastereo- and enantioselective vinylogous Mannich reactions.

Authors: Daniel L Silverio; Peng Fu; Emma L Carswell; Marc L Snapper; Amir H Hoveyda
Journal: Tetrahedron Lett Date: 2015-04-09 Impact factor: 2.415

Review 2. Diastereoselective and enantioselective conjugate addition reactions utilizing α,β-unsaturated amides and lactams.

Authors: Katherine M Byrd
Journal: Beilstein J Org Chem Date: 2015-04-23 Impact factor: 2.883

3. Bifunctional Iminophosphorane-Catalyzed Enantioselective Sulfa-Michael Addition to Unactivated α,β-Unsaturated Amides.

Authors: Daniel Rozsar; Michele Formica; Ken Yamazaki; Trevor A Hamlin; Darren J Dixon
Journal: J Am Chem Soc Date: 2022-01-06 Impact factor: 15.419

4. Lewis Acid Enabled Copper-Catalyzed Asymmetric Synthesis of Chiral β-Substituted Amides.

Authors: Mamen Rodríguez-Fernández; Xingchen Yan; Juan F Collados; Paul B White; Syuzanna R Harutyunyan
Journal: J Am Chem Soc Date: 2017-09-29 Impact factor: 15.419

Review 5. Copper-catalyzed enantioselective conjugate addition of organometallic reagents to challenging Michael acceptors.

Authors: Delphine Pichon; Jennifer Morvan; Christophe Crévisy; Marc Mauduit
Journal: Beilstein J Org Chem Date: 2020-02-17 Impact factor: 2.883

6. Isothiourea-catalysed enantioselective Michael addition of N-heterocyclic pronucleophiles to α,β-unsaturated aryl esters.

Authors: Chang Shu; Honglei Liu; Alexandra M Z Slawin; Cameron Carpenter-Warren; Andrew D Smith
Journal: Chem Sci Date: 2019-10-23 Impact factor: 9.825

6 in total