Enantioselective enolate protonations: Evaluation of achiral templates with fluxional brønsted basic substituents in conjugate addition of malononitriles-Reference-Cited by-同舟云学术

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Enantioselective enolate protonations: Evaluation of achiral templates with fluxional brønsted basic substituents in conjugate addition of malononitriles

Published:2024-02 Issue: Volume:152 Page:133833
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Reimann Sebastian,Adachi Shinya,Subramanian Hariharaputhiran,Sibi Mukund P.^ORCID

Publisher

Elsevier BV

Reference59 articles.

1. Enantioselectively-catalyzed reactions with (E)-2-Alkenoyl-pyridines, their N-Oxides, and the Corresponding Chalcones;Desimoni;Chem. Rev.,2014

2. Substituted (E)-2-Oxo-3-butenoates: Reagents for every enantioselectively-catalyzed reaction;Desimoni;Chem. Rev.,2013

3. Enantioselective catalytic reactions with N-acyliden penta-atomic aza-heterocycles. Heterocycles as masked bricks to build chiral scaffolds;Desimoni;Chem. Rev.,2015

4. Chiral relay: a novel strategy for the control and amplification of enantioselectivity in chiral Lewis acid promoted reactions;Corminboeuf;Chem. Eur J.,2003

5. A new approach to enantiocontrol and enantioselectivity amplification: chiral relay in Diels−Alder reactions;Sibi;J. Am. Chem. Soc.,2001

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