Literature DB >> 18666089

Asymmetric aminocatalysis--gold rush in organic chemistry.

Paolo Melchiorre1, Mauro Marigo, Armando Carlone, Giuseppe Bartoli.   

Abstract

Catalysis with chiral secondary amines (asymmetric aminocatalysis) has become a well-established and powerful synthetic tool for the chemo- and enantioselective functionalization of carbonyl compounds. In the last eight years alone, this field has grown at such an extraordinary pace that it is now recognized as an independent area of synthetic chemistry, where the goal is the preparation of any chiral molecule in an efficient, rapid, and stereoselective manner. This has been made possible by the impressive level of scientific competition and high quality research generated in this area. This Review describes this "Asymmetric Aminocatalysis Gold Rush" and charts the milestones in its development. As in all areas of science, progress depends on human effort.

Entities:  

Year:  2008        PMID: 18666089     DOI: 10.1002/anie.200705523

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  47 in total

Review 1.  Organocatalytic cascade reactions as a new tool in total synthesis.

Authors:  Christoph Grondal; Matthieu Jeanty; Dieter Enders
Journal:  Nat Chem       Date:  2010-02-19       Impact factor: 24.427

2.  The precellular scenario of genovirions.

Authors:  Rolf M Flügel
Journal:  Virus Genes       Date:  2010-04       Impact factor: 2.332

3.  Scaffolding catalysts: highly enantioselective desymmetrization reactions.

Authors:  Xixi Sun; Amanda D Worthy; Kian L Tan
Journal:  Angew Chem Int Ed Engl       Date:  2011-07-07       Impact factor: 15.336

4.  Switchable regioselectivity in amine-catalysed asymmetric cycloadditions.

Authors:  Zhi Zhou; Zhou-Xiang Wang; Yuan-Chun Zhou; Wei Xiao; Qin Ouyang; Wei Du; Ying-Chun Chen
Journal:  Nat Chem       Date:  2017-01-16       Impact factor: 24.427

5.  Synthesis of 9-amino(9-deoxy)epi cinchona alkaloids, general chiral organocatalysts for the stereoselective functionalization of carbonyl compounds.

Authors:  Carlo Cassani; Rafael Martín-Rapún; Elena Arceo; Fernando Bravo; Paolo Melchiorre
Journal:  Nat Protoc       Date:  2013-01-17       Impact factor: 13.491

6.  Direct observation of an enamine intermediate in amine catalysis.

Authors:  Xueyong Zhu; Fujie Tanaka; Richard A Lerner; Carlos F Barbas; Ian A Wilson
Journal:  J Am Chem Soc       Date:  2009-12-30       Impact factor: 15.419

7.  Asymmetric synthesis of 1H-pyrrol-3(2H)-ones from 2,3-diketoesters by combination of aldol condensation with benzilic acid rearrangement.

Authors:  Qiang Sha; Hadi Arman; Michael P Doyle
Journal:  Chem Commun (Camb)       Date:  2016-01-04       Impact factor: 6.222

8.  Catalysis of Hydrogen-Deuterium Exchange Reactions by 4-Substituted Proline Derivatives.

Authors:  Eddie L Myers; Michael J Palte; Ronald T Raines
Journal:  J Org Chem       Date:  2019-01-14       Impact factor: 4.354

9.  Methods for direct alkene diamination, new & old.

Authors:  Sam de Jong; Daniel G Nosal; Duncan J Wardrop
Journal:  Tetrahedron       Date:  2012-03-21       Impact factor: 2.457

10.  Accurate reaction enthalpies and sources of error in DFT thermochemistry for aldol, Mannich, and alpha-aminoxylation reactions.

Authors:  Steven E Wheeler; Antonio Moran; Susan N Pieniazek; K N Houk
Journal:  J Phys Chem A       Date:  2009-09-24       Impact factor: 2.781

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