(Q37435281)

English

Palladium-catalyzed enantioselective alpha-arylation and alpha-vinylation of oxindoles facilitated by an axially chiral P-stereogenic ligand

scientific article published on July 2009

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Palladium-catalyzed enantioselective alpha-arylation and alpha-vinylation of oxindoles facilitated by an axially chiral P-stereogenic ligand (English)

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

enantioselectivity

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

Stephen L. Buchwald

3

object named as

Stephen L Buchwald

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

author name string

Alexander M Taylor

1

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Ryan A Altman

2

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

language of work or name

0 references

publication date

1 July 2009

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Journal of the American Chemical Society

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

131

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

29

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

9900-9901

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

Gelsemine: a thought-provoking target for total synthesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782534

23 August 2017

AcOLeDMAP and BnOLeDMAP: conformationally restricted nucleophilic catalysts for enantioselective rearrangement of indolyl acetates and carbonates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782534

23 August 2017

A highly active catalyst for Pd-catalyzed amination reactions: cross-coupling reactions using aryl mesylates and the highly selective monoarylation of primary amines using aryl chlorides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782534

23 August 2017

Asymmetric palladium-catalyzed intramolecular alpha-arylation of aldehydes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782534

23 August 2017

Orthogonal Pd- and Cu-based catalyst systems for C- and N-arylation of oxindoles.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782534

23 August 2017

A new class of easily activated palladium precatalysts for facile C-N cross-coupling reactions and the low temperature oxidative addition of aryl chlorides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782534

23 August 2017

Enantioselective alpha-arylation of ketones with aryl triflates catalyzed by difluorphos complexes of palladium and nickel

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782534

23 August 2017

Mo-catalyzed regio-, diastereo-, and enantioselective allylic alkylation of 3-aryloxindoles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782534

23 August 2017

Pyrrolidinyl-spirooxindole natural products as inspirations for the development of potential therapeutic agents

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782534

23 August 2017

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=2782534

23 August 2017

BMS-204352: a potassium channel opener developed for the treatment of stroke

1 reference

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23 August 2017

Cinchona alkaloid catalyzed enantioselective fluorination of allyl silanes, silyl enol ethers, and oxindoles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782534

26 June 2018

Enantioselective synthesis of SM-130686 based on the development of asymmetric Cu(I)F catalysis to access 2-oxindoles containing a tetrasubstituted carbon.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782534

2 September 2018

Catalytic enantioselective Meerwein-Eschenmoser Claisen rearrangement: asymmetric synthesis of allyl oxindoles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782534

2 September 2018

Chiral N-heterocyclic carbene ligands for asymmetric catalytic oxindole synthesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782534

2 September 2018

Intermolecular enolate heterocoupling: scope, mechanism, and application

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782534

2 September 2018

Nickel-BINAP catalyzed enantioselective alpha-arylation of alpha-substituted gamma-butyrolactones

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782534

2 September 2018

An improved catalyst for the asymmetric arylation of ketone enolates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2782534

2 September 2018

Catalytic asymmetric vinylation of ketone enolates

1 reference

https://pubmed.ncbi.nlm.nih.gov/19580273

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

P-chirogenic binaphthyl-substituted monophosphines: synthesis and use in enolate vinylation/arylation reactions

1 reference

https://pubmed.ncbi.nlm.nih.gov/19580273

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enantioselective Construction of Quaternary Stereocenters

1 reference

https://pubmed.ncbi.nlm.nih.gov/19580273

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nickel-catalyzed asymmetric alpha-arylation of ketone enolates

1 reference

https://pubmed.ncbi.nlm.nih.gov/19580273

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Palladium-catalyzed alpha-vinylation of carbonyl compounds

1 reference

https://pubmed.ncbi.nlm.nih.gov/19580273

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bulky chiral carbene ligands and their application in the palladium-catalyzed asymmetric intramolecular alpha-arylation of amides

1 reference

https://pubmed.ncbi.nlm.nih.gov/19580273

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Palladium-catalyzed gamma-arylation of beta,gamma-unsaturated ketones: application to a one-pot synthesis of tricyclic indolines

1 reference

https://pubmed.ncbi.nlm.nih.gov/19580273

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enantioselective synthesis of 3,3-disubstituted oxindoles through Pd-catalyzed cyanoamidation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19580273

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Organocatalytic stereoselective mannich reaction of 3-substituted oxindoles

1 reference

https://pubmed.ncbi.nlm.nih.gov/19580273

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Catalytic Enantioselective Construction of Molecules with Quaternary Carbon Stereocenters

1 reference

https://pubmed.ncbi.nlm.nih.gov/19580273

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1021/JA903880Q

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

20 August 2017

ResearchGate publication ID

0 references

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