(Q37104353)

English

Highly(≥98%) Selective Trisubstituted Alkene Synthesis of Wide Applicability via Fluoride-Promoted Pd-Catalyzed Cross-Coupling of Alkenylboranes

scientific article published on December 2010

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Highly(≥98%) Selective Trisubstituted Alkene Synthesis of Wide Applicability via Fluoride-Promoted Pd-Catalyzed Cross-Coupling of Alkenylboranes (English)

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

author name string

Ei-Ichi Negishi

1

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Tomas Tobrman

2

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Honghua Rao

3

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Shiqing Xu

4

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Ching-Tien Lee

5

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

publication date

1 December 2010

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Israel Journal of Chemistry

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

50

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

5-6

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

696-701

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Arylethyne Bromoboration-Negishi Coupling Route to E- or Z-Aryl-Substituted Trisubstituted Alkenes of ≥98% IsomericPurity. New Horizon in the Highly Selective Synthesis of Trisubstituted Alkenes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3747006

14 September 2017

Highly regio- and stereoselective synthesis of (Z)-trisubstituted alkenes via propyne bromoboration and tandem Pd-catalyzed cross-coupling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3747006

14 September 2017

Efficient and stereoselective synthesis of yellow scale pheromone via alkyne haloboration, Zr-catalyzed asymmetric carboalumination of alkenes (ZACA reaction), and Pd-catalyzed tandem Negishi coupling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3747006

14 September 2017

Highly stereoselective synthesis of cis-alkenyl pinacolboronates and potassium cis-alkenyltrifluoroborates via a hydroboration/protodeboronation approach

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3747006

14 September 2017

Palladium complexes of N-heterocyclic carbenes as catalysts for cross-coupling reactions--a synthetic chemist's perspective

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3747006

14 September 2017

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=3747006

14 September 2017

Palladium/P,O-Ligand-Catalyzed Suzuki Cross-Coupling Reactions of Arylboronic Acids and Aryl Chlorides. Isolation and Structural Characterization of (P,O)-Pd(dba) Complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3747006

3 September 2018

Palladium/phosphite catalyst systems for efficient cross coupling of aryl bromides and chlorides with phenylboronic acid

1 reference

https://pubmed.ncbi.nlm.nih.gov/23966749

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Suzuki-Miyaura cross-coupling reactions of potassium alkenyltrifluoroborates

1 reference

https://pubmed.ncbi.nlm.nih.gov/23966749

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clean Inversion of Configuration in the Pd-Catalyzed Cross-Coupling of 2-Bromo-1,3-dienes

1 reference

https://pubmed.ncbi.nlm.nih.gov/23966749

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Highly stereoselective synthesis of (1E)-2-methyl-1,3-dienes by palladium-catalyzed trans-selective cross-coupling of 1,1-dibromo-1-alkenes with alkenylzinc reagents

1 reference

https://pubmed.ncbi.nlm.nih.gov/23966749

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequential Transformations of 1,3-Dibora Butadienes to Enones or Tetrasubstituted 1,3-Butadienes

1 reference

https://pubmed.ncbi.nlm.nih.gov/23966749

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/IJCH.201000051

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

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