Literature DB >> 20419212

The direct catalytic asymmetric aldol reaction.

Barry M Trost1, Cheyenne S Brindle.   

Abstract

Asymmetric aldol reactions are a powerful method for the construction of carbon-carbon bonds in an enantioselective fashion. Historically this reaction has been performed in a stoichiometric fashion to control the various aspects of chemo-, diastereo-, regio- and enantioselectivity, however, a more atom economical approach would unite high selectivity with the use of only a catalytic amount of a chiral promoter. This critical review documents the development of direct catalytic asymmetric aldol methodologies, including organocatalytic and metal-based strategies. New methods have improved the reactivity, selectivity and substrate scope of the direct aldol reaction and enabled the synthesis of complex molecular targets (357 references).

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Year:  2010        PMID: 20419212      PMCID: PMC3714873          DOI: 10.1039/b923537j

Source DB:  PubMed          Journal:  Chem Soc Rev        ISSN: 0306-0012            Impact factor:   54.564


  139 in total

1.  Use of In situ generated ketene in the wynberg beta-lactone synthesis: new transformations of the dichlorinated beta-lactone products

Authors: 
Journal:  J Org Chem       Date:  2000-10-20       Impact factor: 4.354

2.  Direct catalytic asymmetric aldol-type reaction of aldehydes with ethyl diazoacetate.

Authors:  Wengang Yao; Jianbo Wang
Journal:  Org Lett       Date:  2003-05-01       Impact factor: 6.005

3.  New mechanistic studies on the proline-catalyzed aldol reaction.

Authors:  Benjamin List; Linh Hoang; Harry J Martin
Journal:  Proc Natl Acad Sci U S A       Date:  2004-04-08       Impact factor: 11.205

4.  Direct catalytic asymmetric aldol additions of methyl ynones. Spontaneous reversal in the sense of enantioinduction.

Authors:  Barry M Trost; Alec Fettes; Brock T Shireman
Journal:  J Am Chem Soc       Date:  2004-03-10       Impact factor: 15.419

5.  Nonlinear effects in asymmetric synthesis. Examples in asymmetric oxidations and aldolization reactions.

Authors:  C Puchot; O Samuel; E Dunach; S Zhao; C Agami; H B Kagan
Journal:  J Am Chem Soc       Date:  1986-04-01       Impact factor: 15.419

6.  The origin of stereoselectivity in primary amino acid catalyzed intermolecular aldol reactions.

Authors:  Arianna Bassan; Weibiao Zou; Efraim Reyes; Fahmi Himo; Armando Córdova
Journal:  Angew Chem Int Ed Engl       Date:  2005-11-04       Impact factor: 15.336

Review 7.  Asymmetric enamine catalysis.

Authors:  Santanu Mukherjee; Jung Woon Yang; Sebastian Hoffmann; Benjamin List
Journal:  Chem Rev       Date:  2007-12       Impact factor: 60.622

8.  Design and application of linked-BINOL chiral ligands in bifunctional asymmetric catalysis.

Authors:  Masakatsu Shibasaki; Shigeki Matsunaga
Journal:  Chem Soc Rev       Date:  2006-02-09       Impact factor: 54.564

9.  Polystyrene-supported hydroxyproline: an insoluble, recyclable organocatalyst for the asymmetric aldol reaction in water.

Authors:  Daniel Font; Ciril Jimeno; Miquel A Pericàs
Journal:  Org Lett       Date:  2006-09-28       Impact factor: 6.005

10.  Direct catalytic asymmetric aldol reactions of pyruvates: scope and mechanism.

Authors:  Nicholas Gathergood; Karsten Juhl; Thomas B Poulsen; Karl Thordrup; Karl Anker Jørgensen
Journal:  Org Biomol Chem       Date:  2004-03-09       Impact factor: 3.876

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  55 in total

1.  Total synthesis of laulimalide: synthesis of the northern and southern fragments.

Authors:  Barry M Trost; W Michael Seganish; Cheol K Chung; Dominique Amans
Journal:  Chemistry       Date:  2012-02-03       Impact factor: 5.236

2.  The supersilyl group as a carboxylic acid protecting group: application to highly stereoselective aldol and Mannich reactions.

Authors:  Jiajing Tan; Matsujiro Akakura; Hisashi Yamamoto
Journal:  Angew Chem Int Ed Engl       Date:  2013-05-29       Impact factor: 15.336

3.  Generation of stereochemically defined tetrasubstituted enolborinates by 1,4-hydroboration of α,β-unsaturated morpholine carboxamides with (diisopinocampheyl)borane.

Authors:  Christophe Allais; Andy S Tsai; Philippe Nuhant; William R Roush
Journal:  Angew Chem Int Ed Engl       Date:  2013-10-15       Impact factor: 15.336

4.  Separation of Aldehydes and Reactive Ketones from Mixtures Using a Bisulfite Extraction Protocol.

Authors:  Maxwell H Furigay; Maria M Boucher; Nikola A Mizgier; Cheyenne S Brindle
Journal:  J Vis Exp       Date:  2018-04-02       Impact factor: 1.355

Review 5.  Chiral Graphene Hybrid Materials: Structures, Properties, and Chiral Applications.

Authors:  Biao Zhao; Shenghua Yang; Jianping Deng; Kai Pan
Journal:  Adv Sci (Weinh)       Date:  2021-02-12       Impact factor: 16.806

6.  Disparate Catalytic Scaffolds for Atroposelective Cyclodehydration.

Authors:  Yongseok Kwon; Junqi Li; Jolene P Reid; Jennifer M Crawford; Roxane Jacob; Matthew S Sigman; F Dean Toste; Scott J Miller
Journal:  J Am Chem Soc       Date:  2019-04-10       Impact factor: 15.419

7.  Base-catalyzed direct aldolization of α-alkyl-α-hydroxy trialkyl phosphonoacetates.

Authors:  Michael T Corbett; Daisuke Uraguchi; Takashi Ooi; Jeffrey S Johnson
Journal:  Angew Chem Int Ed Engl       Date:  2012-04-04       Impact factor: 15.336

Review 8.  The ever-expanding role of asymmetric covalent organocatalysis in scalable, natural product synthesis.

Authors:  Mikail E Abbasov; Daniel Romo
Journal:  Nat Prod Rep       Date:  2014-10       Impact factor: 13.423

9.  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

10.  Chemo- and regioselective C(sp³)-H arylation of unactivated allylarenes by deprotonative cross-coupling.

Authors:  Nusrah Hussain; Gustavo Frensch; Jiadi Zhang; Patrick J Walsh
Journal:  Angew Chem Int Ed Engl       Date:  2014-02-26       Impact factor: 15.336

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