(Q37968170)

26 August 2017

title

Low-loading asymmetric organocatalysis (English)

1 reference

Michelangelo Gruttadauria

26 August 2017

1 reference

Francesco Giacalone

1

0 references

object named as

Michelangelo Gruttadauria

series ordinal

2

0 references

Renato Noto

object named as

Renato Noto

series ordinal

4

0 references

author name string

Paola Agrigento

series ordinal

3

1 reference

26 August 2017

publication date

14 December 2011

1 reference

26 August 2017

published in

Chemical Society Reviews

1 reference

26 August 2017

volume

41

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26 August 2017

issue

6

1 reference

26 August 2017

page(s)

2406-2447

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In the Golden Age of Organocatalysis

26 August 2017

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Organocatalysis lost: modern chemistry, ancient chemistry, and an unseen biosynthetic apparatus

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Asymmetric organocatalysis: from infancy to adolescence

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The advent and development of organocatalysis

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Organocatalysis--after the gold rush

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Asymmetric organocatalysis in total synthesis--a trial by fire

21 January 2018

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Asymmetric Organocatalytic Domino Reactions

21 January 2018

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Organocatalytic cascade reactions as a new tool in total synthesis

21 January 2018

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Thermodynamic control of asymmetric amplification in amino acid catalysis

21 January 2018

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Spontaneous mirror symmetry breaking in the aldol reaction and its potential relevance in prebiotic chemistry

21 January 2018

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When chiral product and catalyst are the same: discovery of asymmetric organoautocatalysis

21 January 2018

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Enantioselective organocatalytic singly occupied molecular orbital activation: the enantioselective alpha-enolation of aldehydes

21 January 2018

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Merging photoredox catalysis with organocatalysis: the direct asymmetric alkylation of aldehydes

21 January 2018

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A solid-supported organocatalyst for highly stereoselective, batch, and continuous-flow Mannich reactions.

21 January 2018

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5-(Pyrrolidin-2-yl)tetrazole-catalyzed aldol and mannich reactions: acceleration and lower catalyst loading in a continuous-flow reactor

21 January 2018

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Greener approaches to organic synthesis using microreactor technology

21 January 2018

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Organocatalytic reactions in water

21 January 2018

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https://api.crossref.org/works/10.1039%2FC1CS15206H

Fluorine & chirality: how to create a nonracemic stereogenic carbon-fluorine centre?

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Enantioselective organocatalytic synthesis of fluorinated molecules.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Supported proline and proline-derivatives as recyclable organocatalysts

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Recyclable stereoselective catalysts.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Proline-catalyzed asymmetric reactions

21 January 2018

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https://api.crossref.org/works/10.1039%2FC1CS15206H

The ying and yang of asymmetric aminocatalysis

21 January 2018

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https://api.crossref.org/works/10.1039%2FC1CS15206H

21 January 2018

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https://api.crossref.org/works/10.1039%2FC1CS15206H

Asymmetric enamine catalysis

21 January 2018

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https://api.crossref.org/works/10.1039%2FC1CS15206H

Asymmetric aminocatalysis--gold rush in organic chemistry

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Asymmetric synthesis of bicyclic intermediates of natural product chemistry

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

The enantioselective organocatalytic 1,4-addition of electron-rich benzenes to alpha,beta-unsaturated aldehydes

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

The direct and enantioselective organocatalytic alpha-oxidation of aldehydes

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Solid-supported and pegylated H-Pro-Pro-Asp-NHR as catalysts for asymmetric aldol reactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

A highly efficient organocatalyst for direct aldol reactions of ketones with aldehydes [corrected].

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

anti-selective direct asymmetric Mannich reactions catalyzed by axially chiral amino sulfonamide as an organocatalyst

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

A designer axially chiral amino sulfonamide as an efficient organocatalyst for direct asymmetric anti-selective Mannich reactions and syn-selective cross-aldol reactions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

A designer axially chiral amino sulfonamide as an efficient organocatalyst for direct asymmetric mannich reactions of N-Boc-protected imines

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

A general organocatalyst for direct alpha-functionalization of aldehydes: stereoselective C-C, C-N, C-F, C-Br, and C-S bond-forming reactions. Scope and mechanistic insights

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Artificial aldolases from peptide dendrimer combinatorial libraries

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Design of an axially chiral amino acid with a binaphthyl backbone as an organocatalyst for a direct asymmetric aldol reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Direct asymmetric anti-Mannich-type reactions catalyzed by a designed amino acid

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Organocatalytic direct asymmetric aldol reactions in water

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Highly diastereo- and enantioselective direct aldol reactions in water.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Highly diastereo- and enantioselective direct aldol reactions of aldehydes and ketones catalyzed by siloxyproline in the presence of water

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Catalysts based on amino acids for asymmetric reactions in water

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Synthesis of chiral organocatalysts derived from aziridines: application in asymmetric aldol reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

N-(p-dodecylphenylsulfonyl)-2-pyrrolidinecarboxamide: a practical proline mimetic for facilitating enantioselective aldol reactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Chiral enhancement in diethyl malonate addition by morphosynthesized L-proline mesoporous silica

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

An efficient enantioselective method for asymmetric Michael addition of nitroalkanes to alpha,beta-unsaturated aldehydes

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Peptide catalyzed asymmetric conjugate addition reactions of aldehydes to nitroethylene--a convenient entry into gamma2-amino acids

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Tripeptides of the type H-D-Pro-Pro-Xaa-NH2 as catalysts for asymmetric 1,4-addition reactions: structural requirements for high catalytic efficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Water-compatible iminium activation: organocatalytic Michael reactions of carbon-centered nucleophiles with enals

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Asymmetric formal trans-dihydroxylation and trans-aminohydroxylation of alpha,beta-unsaturated aldehydes via an organocatalytic reaction cascade

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Organocatalytic preparation of simple β-hydroxy and β-amino esters: low catalyst loadings and gram-scale synthesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Asymmetric organocatalysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Enantioselective Mannich-type reaction catalyzed by a chiral Brønsted acid

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Chiral Brønsted acid-catalyzed direct Mannich reactions via electrophilic activation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Organocatalytic asymmetric aza-Friedel-Crafts alkylation of furan.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Chiral Brønsted acid-catalyzed enantioselective alpha-hydroxylation of beta-dicarbonyl compounds.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

A highly enantioselective Brønsted acid catalyzed cascade reaction: organocatalytic transfer hydrogenation of quinolines and their application in the synthesis of alkaloids

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

The development of double axially chiral phosphoric acids and their catalytic transfer hydrogenation of quinolines

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Asymmetric synthesis of indolines by catalytic enantioselective reduction of 3H-indoles

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Asymmetric transfer hydrogenation of beta,gamma-alkynyl alpha-imino esters by a Brønsted acid.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Highly enantioselective hydrogenation of enamides catalyzed by chiral phosphoric acids

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Activation of hemiaminal ethers by chiral Brønsted acids for facile access to enantioselective two-carbon homologation using enecarbamates

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Double bond isomerization/enantioselective aza-Petasis-Ferrier rearrangement sequence as an efficient entry to anti- and enantioenriched beta-amino aldehydes

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Chiral Brønsted acid catalyzed pinacol rearrangement.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

A Brønsted acid catalyst for the enantioselective protonation reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Pyridinium 1,1'-binaphthyl-2,2'-disulfonates as highly effective chiral Brønsted acid-base combined salt catalysts for enantioselective Mannich-type reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Chiral guanidine catalyzed enantioselective reactions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Asymmetric organocatalysis by chiral Brønsted bases: implications and applications

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

A highly enantioselective and general conjugate addition of thiols to cyclic enones with an organic catalyst

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Asymmetric Michael addition of trisubstituted carbanion to nitroalkenes catalyzed by sodium demethylquinine salt in water

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Organocatalytic sequential Michael reactions: stereoselective synthesis of multifunctionalized tetrahydroindan derivatives

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Catalytic enantioselective synthesis of alpha,beta-diamino acid derivatives.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Asymmetric Catalysis of the Strecker Amino Acid Synthesis by a Cyclic Dipeptide

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Enantioselective 1,4-addition reactions of diphenyl phosphite to nitroalkenes catalyzed by an axially chiral guanidine

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Chiral ammonium betaines: a bifunctional organic base catalyst for asymmetric Mannich-type reaction of alpha-nitrocarboxylates.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Flexible synthesis, structural determination, and synthetic application of a new C1-symmetric chiral ammonium betaine

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Chiral tetraaminophosphonium carboxylate-catalyzed direct Mannich-type reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Chiral organic ion pair catalysts assembled through a hydrogen-bonding network.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

A Powerful Chiral Counteranion Motif for Asymmetric Catalysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Lewis Base Catalysis in Organic Synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Recent progress in Lewis base activation and control of stereoselectivity in the additions of trimethylsilyl nucleophiles.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

A new synthetic route to enantiomerically pure axially chiral 2,2'-bipyridine N,N'-dioxides. Highly efficient catalysts for asymmetric allylation of aldehydes with allyl(trichloro)silanes

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Lewis base activation of lewis acids. Addition of silyl ketene acetals to aldehydes

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Lewis base activation of Lewis acids: catalytic, enantioselective addition of glycolate-derived silyl ketene acetals to aldehydes

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

N-silyl oxyketene imines are underused yet highly versatile reagents for catalytic asymmetric synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Catalytic asymmetric cyanosilylation of ketones with chiral Lewis base

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Asymmetric reduction of ketimines with trichlorosilane employing an imidazole derived organocatalyst

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Metal-free organocatalysis through explicit hydrogen bonding interactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Activation of carbonyl compounds by double hydrogen bonding: an emerging tool in asymmetric catalysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Recognition and activation by ureas and thioureas: stereoselective reactions using ureas and thioureas as hydrogen-bonding donors

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

"Designer acids": combined acid catalysis for asymmetric synthesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Asymmetric catalysis by chiral hydrogen-bond donors

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Small-molecule H-bond donors in asymmetric catalysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Hydrogen-bond-mediated asymmetric catalysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Asymmetric catalysis with bifunctional cinchona alkaloid-based urea and thiourea organocatalysts

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Development of chiral thiourea catalysts and its application to asymmetric catalytic reactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Schiff Base Catalysts for the Asymmetric Strecker Reaction Identified and Optimized from Parallel Synthetic Libraries

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

A General Catalyst for the Asymmetric Strecker Reaction This work was supported by the NIH (GM-43214). A postdoctoral fellowship to M.S.S. (NIH), and a predoctoral fellowship to P.V. sponsored by Alfred Bader are gratefully acknowledged

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Structure-based analysis and optimization of a highly enantioselective catalyst for the strecker reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Enantioselective organocatalytic direct Michael addition of nitroalkanes to nitroalkenes promoted by a unique bifunctional DMAP-thiourea

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

The mechanism and an improved asymmetric allylboration of ketones catalyzed by chiral biphenols

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Chiral amine-thioureas bearing multiple hydrogen bonding donors: highly efficient organocatalysts for asymmetric Michael addition of acetylacetone to nitroolefins

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Direct organocatalytic asymmetric aldol reaction of alpha-isothiocyanato imides to alpha-ketoesters under low ligand loading: a doubly stereocontrolled approach to cyclic thiocarbamates bearing chiral quaternary stereocenters.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Urea- and thiourea-substituted cinchona alkaloid derivatives as highly efficient bifunctional organocatalysts for the asymmetric addition of malonate to nitroalkenes: inversion of configuration at C9 dramatically improves catalyst performance

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Highly enantioselective desymmetrization of meso anhydrides by a bifunctional thiourea-based organocatalyst at low catalyst loadings and room temperature

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Squaramides: physical properties, synthesis and applications

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Chiral squaramide derivatives are excellent hydrogen bond donor catalysts

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Chiral squaramides as highly enantioselective catalysts for Michael addition reactions of 4-hydroxycoumarins and 4-hydroxypyrone to beta,gamma-unsaturated alpha-keto esters

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Squaramide-catalyzed enantioselective Friedel-Crafts reaction of indoles with imines

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Enantioselective alpha-amination of 1,3-dicarbonyl compounds using squaramide derivatives as hydrogen bonding catalysts

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Recent advances in asymmetric phase-transfer catalysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Enantioselective amino acid synthesis by chiral phase-transfer catalysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Recent development and application of chiral phase-transfer catalysts

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Organocatalytic asymmetric conjugate addition to allenic esters and ketones

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Chiral bifunctional phase transfer catalysts for asymmetric fluorination of beta-keto esters

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Phase-transfer-catalyzed asymmetric alkylation of alpha-benzoyloxy-beta-keto esters: stereoselective construction of congested 2,3-dihydroxycarboxylic acid esters

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Site-directed asymmetric quaternization of a peptide backbone at a C-terminal azlactone

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Organocatalysis by N-heterocyclic carbenes

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Chiral N-heterocyclic carbene catalyzed, enantioselective oxodiene Diels-Alder reactions with low catalyst loadings

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Light in aminocatalysis: the asymmetric intermolecular alpha-alkylation of aldehydes

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Organocatalytic reactions: effects of ball milling, microwave and ultrasound irradiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Amino acids and peptides as asymmetric organocatalysts

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Thermal Effects in the Organocatalytic Asymmetric Mannich Reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Nucleophilic Chiral Amines as Catalysts in Asymmetric Synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Asymmetric Michael addition of α-nitro-ketones using catalytic peptides

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Protonated Chiral Catalysts: Versatile Tools for Asymmetric Synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Synthesis of Enantiopure (S)-Indolylglycine by Organocatalyzed Friedel–Crafts Alkylation of Indole

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Organocatalytic Enantioselective Total Synthesis of (−)-Arboricine

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Catalytic Asymmetric Acylcyanation of Imines

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

Application of Chiral Ionic Liquids for Asymmetric Induction in Catalysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1039%2FC1CS15206H

21 January 2018

Identifiers

DOI

10.1039/C1CS15206H

1 reference

release_wvqyfipx4zasvhxn23ejcy6mxi

26 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/wvqyfipx4zasvhxn23ejcy6mxi

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference