(Q42680516)

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Asymmetric synthesis of functionalized cyclopentanones via a multicatalytic secondary amine/N-heterocyclic carbene catalyzed cascade sequence

scientific article published on September 2009

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

4 November 2017

Asymmetric synthesis of functionalized cyclopentanones via a multicatalytic secondary amine/N-heterocyclic carbene catalyzed cascade sequence (English)

1 reference

Europe PubMed Central

PMC publication ID

4 November 2017

2

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Tomislav Rovis

1 reference

Europe PubMed Central

PMC publication ID

4 November 2017

author name string

Stephen P Lathrop

1

1 reference

Europe PubMed Central

PMC publication ID

4 November 2017

language of work or name

0 references

publication date

1 September 2009

1 reference

Europe PubMed Central

PMC publication ID

4 November 2017

Journal of the American Chemical Society

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Europe PubMed Central

PMC publication ID

4 November 2017

131

1 reference

Europe PubMed Central

PMC publication ID

4 November 2017

38

1 reference

Europe PubMed Central

PMC publication ID

4 November 2017

13628-13630

1 reference

Europe PubMed Central

PMC publication ID

4 November 2017

The Catalytic Asymmetric Intramolecular Stetter Reaction

1 reference

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27 May 2018

Achieving molecular complexity by organocatalytic one-pot strategies - a fast entry for synthesis of sphingoids, amino sugars, and polyhydroxylated alpha-amino acids

1 reference

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27 May 2018

Cycle-specific organocascade catalysis: application to olefin hydroamination, hydro-oxidation, and amino-oxidation, and to natural product synthesis

1 reference

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27 May 2018

High-yielding synthesis of the anti-influenza neuramidase inhibitor (-)-oseltamivir by three "one-pot" operations

1 reference

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27 May 2018

Nucleophilic carbene catalyzed synthesis of 1,2 amino alcohols via azidation of epoxy aldehydes

1 reference

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27 May 2018

Organocatalysis: asymmetric cascade reactions catalysed by chiral secondary amines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785226

27 May 2018

Asymmetric enamine catalysis

1 reference

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27 May 2018

Iminium catalysis

1 reference

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27 May 2018

Organocatalysis by N-heterocyclic carbenes

1 reference

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27 May 2018

Asymmetric Organocatalytic Domino Reactions

1 reference

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27 May 2018

Catalytic enantioselective crossed aldehyde-ketone benzoin cyclization.

1 reference

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27 May 2018

Asymmetric intramolecular crossed-benzoin reactions by N-heterocyclic carbene catalysis

1 reference

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27 May 2018

Enantioselective organo-cascade catalysis

1 reference

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27 May 2018

An efficient synthesis of achiral and chiral 1,2,4-triazolium salts: bench stable precursors for N-heterocyclic carbenes

1 reference

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27 May 2018

Concurrent tandem catalysis

1 reference

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27 May 2018

Cooperative multi-catalyst systems for one-pot organic transformations

1 reference

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27 May 2018

Organocatalytic asymmetric Michael reaction of cyclic 1,3-dicarbonyl compounds and alpha,beta-unsaturated ketones--a highly atom-economic catalytic one-step formation of optically active warfarin anticoagulant

1 reference

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27 May 2018

Multicatalytic synthesis of alpha-pyrrolidinyl ketones via a tandem palladium(II)/indium(III)-catalyzed aminochlorocarbonylation/Friedel-Crafts acylation reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785226

16 August 2018

Nucleophilic carbene and HOAt relay catalysis in an amide bond coupling: an orthogonal peptide bond forming reaction

1 reference

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16 August 2018

Asymmetric organocatalytic conjugate addition of malonates to enones using a proline tetrazole catalyst

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785226

16 August 2018

Enantioselective protonation of catalytically generated chiral enolates as an approach to the synthesis of alpha-chloroesters

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785226

16 August 2018

Diphenylprolinol silyl ethers as efficient organocatalysts for the asymmetric Michael reaction of aldehydes and nitroalkenes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785226

16 August 2018

Asymmetric organic catalysis with modified cinchona alkaloids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785226

16 August 2018

Catalytic generation of activated carboxylates: direct, stereoselective synthesis of beta-hydroxyesters from epoxyaldehydes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785226

16 August 2018

Catalytic intramolecular crossed aldehyde--ketone benzoin reactions: a novel synthesis of functionalized preanthraquinones

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785226

16 August 2018

Modified Chiral Triazolium Salts for Enantioselective Benzoin Cyclization of Enolizable Keto-Aldehydes: Synthesis of (+)-Sappanone B

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2785226

1 December 2018

One-pot organocatalytic domino Michael-aldol and intramolecular SN2 reactions. Asymmetric synthesis of highly functionalized epoxycyclohexanone derivatives

1 reference

https://pubmed.ncbi.nlm.nih.gov/19731910

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A New Approach for an Organocatalytic Multicomponent Domino Asymmetric Reaction

1 reference

https://pubmed.ncbi.nlm.nih.gov/19731910

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple asymmetric organocatalytic approach to optically active cyclohexenones

1 reference

https://pubmed.ncbi.nlm.nih.gov/19731910

12 December 2020

based on heuristic

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Asymmetric Organocatalytic Domino Michael/Aldol Reactions: Enantioselective Synthesis of Chiral Cycloheptanones, Tetrahydrochromenones, and Polyfunctionalized Bicyclo[3.2.1]octanes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19731910

12 December 2020

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inferred from PubMed ID database lookup

Catalytic asymmetric oxa-Michael-Michael cascade for facile construction of chiral chromans via an aminal intermediate

1 reference

https://pubmed.ncbi.nlm.nih.gov/19731910

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inferred from PubMed ID database lookup

N-heterocyclic carbene-catalyzed generation of homoenolates: gamma-butyrolactones by direct annulations of enals and aldehydes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19731910

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Highly enantio- and diastereoselective organocatalytic asymmetric domino Michael-aldol reaction of beta-ketoesters and alpha,beta-unsaturated ketones

1 reference

https://pubmed.ncbi.nlm.nih.gov/19731910

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Control of four stereocentres in a triple cascade organocatalytic reaction

1 reference

https://pubmed.ncbi.nlm.nih.gov/19731910

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Highly enantioselective organocatalytic conjugate addition of malonates to acyclic alpha,beta-unsaturated enones

1 reference

https://pubmed.ncbi.nlm.nih.gov/19731910

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two birds with one metallic stone: single-pot catalysis of fundamentally different transformations

1 reference

https://pubmed.ncbi.nlm.nih.gov/19731910

12 December 2020

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inferred from PubMed ID database lookup

Asymmetric Organocatalysis: An Efficient Enantioselective Access to Benzopyranes and Chromenes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19731910

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based on heuristic

inferred from PubMed ID database lookup

Synthesis of highly functionalized chiral cyclopentanes by catalytic enantio- and diastereoselective double Michael addition reactions

1 reference

https://pubmed.ncbi.nlm.nih.gov/19731910

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diphenylprolinol silyl ether catalysis in an asymmetric formal carbo [3 + 3] cycloaddition reaction via a domino Michael/Knoevenagel condensation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19731910

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Conversion of alpha-haloaldehydes into acylating agents by an internal redox reaction catalyzed by nucleophilic carbenes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19731910

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based on heuristic

inferred from PubMed ID database lookup

Enantioselective organocatalyzed alpha sulfenylation of aldehydes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19731910

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based on heuristic

inferred from PubMed ID database lookup

Organocatalytic conjugate addition of malonates to alpha,beta-unsaturated aldehydes: asymmetric formal synthesis of (-)-paroxetine, chiral lactams, and lactones

1 reference

https://pubmed.ncbi.nlm.nih.gov/19731910

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Organocatalytic enantioselective cascade Michael-aldol condensation reactions: efficient assembly of densely functionalized chiral cyclopentenes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19731910

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catalytic generation of activated carboxylates from enals: a product-determining role for the base

1 reference

https://pubmed.ncbi.nlm.nih.gov/19731910

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1021/JA905342E

1 reference

Europe PubMed Central

PMC publication ID

4 November 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

4 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

4 November 2017

ResearchGate publication ID

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