Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions of Enantiomerically Enriched Potassium β-Trifluoroboratoamides with Various Aryl- and Hetaryl Chlorides (Q42088948)

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scientific article published on October 1, 2010

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English	Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions of Enantiomerically Enriched Potassium β-Trifluoroboratoamides with Various Aryl- and Hetaryl Chlorides	scientific article published on October 1, 2010

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scholarly article

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Europe PubMed Central

PMC publication ID

16 October 2017

Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions of enantiomerically enriched potassium β-trifluoroboratoamides with various aryl- and hetaryl chlorides (English)

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions of Enantiomerically Enriched Potassium β-Trifluoroboratoamides with Various Aryl- and Hetaryl Chlorides (English)

1 reference

10.1021/OL101865E

https://api.crossref.org/works/10.1021/OL101865E

10 July 2024

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Gary A. Molander

1

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Gary A Molander

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16 October 2017

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Inji Shin

2

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Europe PubMed Central

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16 October 2017

Ludivine Jean-Gérard

3

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16 October 2017

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1 October 2010

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Europe PubMed Central

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16 October 2017

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10 July 2024

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20831191/pdf/?tool=EBI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20831191

10 July 2024

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20831191/?tool=EBI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20831191

10 July 2024

https://europepmc.org/articles/PMC2946850

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20831191

10 July 2024

https://europepmc.org/articles/PMC2946850?pdf=render

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Europe PubMed Central

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20831191

10 July 2024

https://doi.org/10.1021/ol101865e

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10 July 2024

https://pubs.acs.org/doi/pdf/10.1021/ol101865e

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10.1021/OL101865E

https://api.crossref.org/works/10.1021/OL101865E

10 July 2024

Organic Letters

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Europe PubMed Central

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16 October 2017

12

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Europe PubMed Central

PMC publication ID

16 October 2017

19

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Europe PubMed Central

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16 October 2017

4384-4387

1 reference

Europe PubMed Central

PMC publication ID

16 October 2017

Organotrifluoroborates and monocoordinated palladium complexes as catalysts--a perfect combination for Suzuki-Miyaura coupling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2946850

29 May 2018

Potassium trifluoroborate salts as convenient, stable reagents for difficult alkyl transfers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2946850

29 May 2018

Use of potassium beta-trifluoroborato amides in Suzuki-Miyaura cross-coupling reactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2946850

29 May 2018

Scope of the Suzuki-Miyaura cross-coupling reaction of potassium trifluoroboratoketohomoenolates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2946850

29 May 2018

Potassium organotrifluoroborates: new perspectives in organic synthesis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2946850

29 May 2018

Organotrifluoroborates: protected boronic acids that expand the versatility of the Suzuki coupling reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2946850

29 May 2018

Enantioselective rhodium enolate protonations. A new methodology for the synthesis of beta2-amino acids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2946850

29 May 2018

Palladium-catalyzed coupling reactions of aryl chlorides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2946850

29 May 2018

Access to enantioenriched alpha-amino esters via rhodium-catalyzed 1,4-addition/enantioselective protonation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2946850

17 August 2018

Rhodium catalysed tandem conjugate addition-protonation: an enantioselective synthesis of 2-substituted succinic esters

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2946850

17 August 2018

Highly Enantioselective Synthesis of Optically Active Ketones by Iridium-Catalyzed Asymmetric Hydrogenation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2946850

1 December 2018

Rhodium-catalysed addition of organotrialkoxysilanes to alpha-substituted acrylic esters

1 reference

https://pubmed.ncbi.nlm.nih.gov/20831191

12 December 2020

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Iridium-catalyzed highly enantioselective hydrogenation of the C=C bond of alpha, beta-unsaturated ketones

1 reference

https://pubmed.ncbi.nlm.nih.gov/20831191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tandem 1,4-addition/enantioselective protonation catalyzed by rhodium complexes: efficient access to alpha-amino acids

1 reference

https://pubmed.ncbi.nlm.nih.gov/20831191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Racemization in suzuki couplings: a quantitative study using 4-hydroxyphenylglycine and tyrosine derivatives as probe molecules

1 reference

https://pubmed.ncbi.nlm.nih.gov/20831191

12 December 2020

based on heuristic

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Rhodium-Catalyzed Conjugate Addition−Enantioselective Protonation: The Synthesis of α,α‘-Dibenzyl Esters

1 reference

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12 December 2020

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A convenient, NMR-based method for the analysis of diastereomeric mixtures of pseudoephedrine amides

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Total synthesis and antitumor activity of 12,13-desoxyepothilone F: an unexpected solvolysis problem at C15, mediated by remote substitution at C21

1 reference

https://pubmed.ncbi.nlm.nih.gov/20831191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Suzuki-Miyaura cross-coupling of potassium trifluoroboratohomoenolates

1 reference

https://pubmed.ncbi.nlm.nih.gov/20831191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Iridium-catalyzed enantioselective hydrogenation of alpha,beta-unsaturated carboxylic acids

1 reference

https://pubmed.ncbi.nlm.nih.gov/20831191

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Asymmetric 1,4 addition of Grignard reagents to chiral α,β-unsaturated esters in the presence of Lewis acids

11

1 reference

10.1021/OL101865E

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10 July 2024

Palladium-Catalyzed Cross-Coupling Reactions of Organoboron Compounds

20

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10.1021/OL101865E

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10 July 2024

Aldrichimica Acta

24

38

49

author name string

Molander G. A.

publication date

2005

1 reference

10.1021/OL101865E

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10 July 2024

Pseudoephedrine as a Practical Chiral Auxiliary for the Synthesis of Highly Enantiomerically Enriched Carboxylic Acids, Alcohols, Aldehydes, and Ketones

34

1 reference

10.1021/OL101865E

https://api.crossref.org/works/10.1021/OL101865E

10 July 2024

Identifiers

10.1021/OL101865E

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

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