(Q42066623)

English

Enantioselective synthesis of alpha,alpha-disubstituted cyclopentenes by an N-heterocyclic carbene-catalyzed desymmetrization of 1,3-diketones

scientific article published on 31 July 2007

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

Enantioselective synthesis of alpha,alpha-disubstituted cyclopentenes by an N-heterocyclic carbene-catalyzed desymmetrization of 1,3-diketones (English)

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

enantioselectivity

1 reference

based on heuristic

inferred from title

4

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

author name string

Manabu Wadamoto

1

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

Eric M Phillips

2

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

Troy E Reynolds

3

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

language of work or name

0 references

publication date

31 July 2007

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

Journal of the American Chemical Society

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

129

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

33

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

10098-10099

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

Highly stereoselective formal [3 + 3] cycloaddition of enals and azomethine imines catalyzed by N-heterocyclic carbenes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3059850

5 June 2018

A highly enantioselective intramolecular Michael reaction catalyzed by N-heterocyclic carbenes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3059850

5 June 2018

Asymmetric synthesis of hydrobenzofuranones via desymmetrization of cyclohexadienones using the intramolecular Stetter reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3059850

5 June 2018

Catalytic enantioselective thioester aldol reactions that are compatible with protic functional groups

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3059850

5 June 2018

Enantioselective enzymatic desymmetrizations in organic synthesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3059850

5 June 2018

Asymmetric multicomponent reactions (AMCRs): the new frontier

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3059850

5 June 2018

Catalytic asymmetric synthesis of all-carbon quaternary stereocenters

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3059850

5 June 2018

Enantioselective, cyclopentene-forming annulations via NHC-catalyzed benzoin-oxy-cope reactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3059850

17 August 2018

Highly enantioselective azadiene Diels-Alder reactions catalyzed by chiral N-heterocyclic carbenes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3059850

17 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=3059850

17 August 2018

Catalytic conjugate additions of carbonyl anions under neutral aqueous conditions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3059850

17 August 2018

Catalytic decarboxylative sp-sp3 coupling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3059850

17 August 2018

Regio- and enantioselective Pd-catalyzed allylic alkylation of ketones through allyl enol carbonates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3059850

17 August 2018

The enantioselective Tsuji allylation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3059850

17 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=3059850

17 August 2018

The thiazolium-catalyzed Sila-Stetter reaction: conjugate addition of acylsilanes to unsaturated esters and ketones

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3059850

17 August 2018

Nucleophilic Chiral Amines as Catalysts in Asymmetric Synthesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3059850

1 December 2018

Tandem oxidation of allylic and benzylic alcohols to esters catalyzed by N-heterocyclic carbenes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17663558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The enantioselective synthesis of alpha-amino acids by phase-transfer catalysis with achiral Schiff base esters

1 reference

https://pubmed.ncbi.nlm.nih.gov/17663558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Practical, catalytic, asymmetric synthesis of beta-lactones via a sequential ketene dimerization/hydrogenation process: inhibitors of the thioesterase domain of fatty acid synthase

1 reference

https://pubmed.ncbi.nlm.nih.gov/17663558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catalytic additions of acylsilanes to imines: an acyl anion strategy for the direct synthesis of alpha-amino ketones

1 reference

https://pubmed.ncbi.nlm.nih.gov/17663558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Conversion of alpha,beta-unsaturated aldehydes into saturated esters: an Umpolung reaction catalyzed by nucleophilic carbenes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17663558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

N-heterocyclic carbene-catalyzed reaction of chalcones and enals via homoenolate: an efficient synthesis of 1,3,4-trisubstituted cyclopentenes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17663558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ruthenium-catalyzed decarboxylative allylation of nonstabilized ketone enolates

1 reference

https://pubmed.ncbi.nlm.nih.gov/17663558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intramolecular, nucleophile-catalyzed aldol-lactonization (NCAL) reactions: catalytic, asymmetric synthesis of bicyclic beta-lactones

1 reference

https://pubmed.ncbi.nlm.nih.gov/17663558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Asymmetric alcoholysis of cyclic anhydrides

1 reference

https://pubmed.ncbi.nlm.nih.gov/17663558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hydroacylation of activated ketones catalyzed by N-heterocyclic carbenes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17663558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1021/JA073987E

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

ResearchGate publication ID

0 references

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