Haloboration of internal alkynes with boronium and borenium cations as a route to tetrasubstituted alkenes (Q42562828)

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scientific article published on 5 June 2013

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English	Haloboration of internal alkynes with boronium and borenium cations as a route to tetrasubstituted alkenes	scientific article published on 5 June 2013

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instance of

scholarly article

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Europe PubMed Central

PMC publication ID

3749439

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2 November 2017

title

Haloboration of internal alkynes with boronium and borenium cations as a route to tetrasubstituted alkenes (English)

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Europe PubMed Central

PMC publication ID

3749439

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2 November 2017

author

Michael J. Ingleson

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5

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Europe PubMed Central

PMC publication ID

3749439

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2 November 2017

Ewan R Clark

object named as

Ewan R Clark

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2

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Ian A Cade

object named as

Ian A Cade

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3

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author name string

James R Lawson

series ordinal

1

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Europe PubMed Central

PMC publication ID

3749439

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2 November 2017

Sophia A Solomon

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4

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Europe PubMed Central

PMC publication ID

3749439

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2 November 2017

language of work or name

English

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publication date

5 June 2013

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Europe PubMed Central

PMC publication ID

3749439

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2 November 2017

published in

Angewandte Chemie International Edition

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volume

52

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Europe PubMed Central

PMC publication ID

3749439

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2 November 2017

issue

29

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Europe PubMed Central

PMC publication ID

3749439

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2 November 2017

page(s)

7518-7522

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Europe PubMed Central

PMC publication ID

3749439

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2 November 2017

cites work

Borenium ion catalyzed hydroboration of alkenes with N-heterocyclic carbene-boranes

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3749439

retrieved

28 May 2018

Cationic tricoordinate boron intermediates: borenium chemistry from the organic perspective

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3749439

retrieved

28 May 2018

A Boronium Ion with Exceptional Electrophilicity

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3749439

retrieved

28 May 2018

Borostannylation of alkynes and enynes. Scope and limitations of the reaction and utility of the adducts

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3749439

retrieved

28 May 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3749439

retrieved

28 May 2018

Borinium, borenium, and boronium ions: synthesis, reactivity, and applications

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3749439

retrieved

28 May 2018

The hydride-ion affinity of borenium cations and their propensity to activate H2 in frustrated Lewis pairs

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3749439

retrieved

16 August 2018

Palladium(0)-catalyzed cross-coupling of potassium (Z)-2-chloroalk-1-enyl trifluoroborates: a chemo- and stereoselective access to (Z)-chloroolefins and trisubstituted alkenes.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3749439

retrieved

16 August 2018

Identification of a boron-containing intermediate in the boron tribromide mediated aryl propargyl ether cleavage reaction

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3749439

retrieved

16 August 2018

Palladium-catalyzed carboboration of alkynes using chloroborane and organozirconium reagents

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3749439

retrieved

16 August 2018

Palladium-catalyzed trans- and cis-carboboration of alkynes tethered to chloroborane with organozirconium reagents: ligand-dependent complementary stereoselectivity

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3749439

retrieved

16 August 2018

Nickel-catalyzed trans-alkynylboration of alkynes via activation of a boron-chlorine bond

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3749439

retrieved

16 August 2018

Isolation of an intermediate in the insertion of a carbodiimide into a boron-aryl bond

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3749439

retrieved

16 August 2018

Stereoselective cross-coupling reaction of 1,1-Diboryl-1-alkenes with electrophiles: a highly stereocontrolled approach to 1,1,2-triaryl-1-alkenes

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3749439

retrieved

16 August 2018

Palladium-catalyzed addition of cyanoboranes to alkynes: regio- and stereoselective synthesis of alpha,beta-unsaturated beta-boryl nitriles.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3749439

retrieved

16 August 2018

Palladium- and nickel-catalyzed intramolecular cyanoboration of alkynes.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3749439

retrieved

16 August 2018

The chemistry of borinium and borenium ions

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FANIE.201302609

retrieved

21 January 2018

Frustrated Lewis Pairs: Metal-free Hydrogen Activation and More

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2FANIE.201302609

retrieved

21 January 2018

Copper-catalyzed three-component carboboration of alkynes and alkenes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/23740843

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Simple inexpensive boron electrophiles for direct arene borylation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/23740843

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanistic Studies into Amine-Mediated Electrophilic Arene Borylation and Its Application in MIDA Boronate Synthesis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/23740843

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Borylcyanocuprate in a one-pot carboboration by a sequential reaction with an electron-deficient alkyne and an organic carbon electrophile

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/23740843

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Geminal Difunctionalization of Alkenylidene-Type Carbenoids by Using Interelement Compounds

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/23740843

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Stereocontrolled synthesis of tetrasubstituted olefins

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/23740843

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1,1-Carboboration

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/23740843

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Copper(I)-Catalyzed Formal Carboboration of Alkynes: Synthesis of Tri- and Tetrasubstituted Vinylboronates

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/23740843

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reaction of Frustrated Lewis Pairs with Conjugated Ynones‐Selective Hydrogenation of the Carbon–Carbon Triple Bond

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/23740843

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Copper-catalyzed three-component borylstannylation of alkynes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/23740843

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Signal‐Enhanced Liquid‐Crystal DNA Biosensors Based on Enzymatic Metal Deposition

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/23740843

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Terminal alkyne activation by frustrated and classical Lewis acid/phosphine pairs

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/23740843

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catalytic carboborations

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/23740843

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1002/ANIE.201302609

1 reference

stated in

Europe PubMed Central

PMC publication ID

3749439

retrieved

2 November 2017

PMC publication ID

3749439

1 reference

stated in

Europe PubMed Central

PMC publication ID

3749439

retrieved

2 November 2017

PubMed publication ID

23740843

1 reference

stated in

Europe PubMed Central

PMC publication ID

3749439

retrieved

2 November 2017

ResearchGate publication ID

237060624

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