(Q37193719)

English

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

scientific article published on March 2010

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scholarly article

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 (English)

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

author name string

Chao Wang

1

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Zhaoqing Xu

2

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Tomas Tobrman

3

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Ei-Ichi Negishi

4

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

publication date

1 March 2010

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

Advanced Synthesis & Catalysis

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

352

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

4

1 reference

Europe PubMed Central

PMC publication ID

18 August 2017

627-631

1 reference

Europe PubMed Central

PMC publication ID

18 August 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=3781582

6 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=3781582

6 September 2017

Efficient and selective syntheses of (all-E)- and (6E,10Z)-2'-O-methylmyxalamides D via Pd-catalyzed alkenylation--carbonyl olefination synergy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781582

6 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=3781582

6 September 2017

The first general method for palladium-catalyzed Negishi cross-coupling of aryl and vinyl chlorides: use of commercially available Pd(P(t-Bu)(3))(2) as a catalyst.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781582

3 September 2018

Highly selective synthesis of (E)-3-methyl-1-trialkylsilyl-3-en-1-ynes via trans-selective alkynylation catalyzed by Cl2Pd(DPEphos) and stereospecific methylation with methylzincs catalyzed by Pd(tBu3P)2

1 reference

https://pubmed.ncbi.nlm.nih.gov/24072992

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new reaction of aryl aldehydes with aryl acetylenes in the presence of boron trihalides

1 reference

https://pubmed.ncbi.nlm.nih.gov/24072992

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Substitution of benzylic hydroxyl groups with vinyl moieties using vinylboron dihalides

1 reference

https://pubmed.ncbi.nlm.nih.gov/24072992

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/24072992

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alkenylation of allylic alcohols using alkenylboron dihalides: a formal transition-metal free Suzuki reaction

1 reference

https://pubmed.ncbi.nlm.nih.gov/24072992

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/ADSC.200900766

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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