Pinene-derived iminodiacetic acid (PIDA): a powerful ligand for stereoselective synthesis and iterative cross-coupling of C(sp3) boronate building blocks (Q38273207)

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English	Pinene-derived iminodiacetic acid (PIDA): a powerful ligand for stereoselective synthesis and iterative cross-coupling of C(sp3) boronate building blocks	scientific article

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

Pinene-derived iminodiacetic acid (PIDA): a powerful ligand for stereoselective synthesis and iterative cross-coupling of C(sp3) boronate building blocks (English)

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

stereoselectivity

1 reference

based on heuristic

inferred from title

author name string

Junqi Li

1

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

Martin D Burke

2

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Europe PubMed Central

PMC publication ID

1 September 2017

language of work or name

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publication date

10 August 2011

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Europe PubMed Central

PMC publication ID

1 September 2017

Journal of the American Chemical Society

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Europe PubMed Central

PMC publication ID

1 September 2017

133

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Europe PubMed Central

PMC publication ID

1 September 2017

35

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

13774-13777

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

Tandem Cycloisomerization/Suzuki Coupling of Arylethynyl MIDA Boronates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

6 September 2017

One-pot reductive amination and Suzuki-Miyaura cross-coupling of formyl aryl and heteroaryl MIDA boronates in array format

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

6 September 2017

Synthesis of atropisomerically defined, highly substituted biaryl scaffolds through catalytic enantioselective bromination and regioselective cross-coupling

1 reference

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6 September 2017

Asymmetric alkyl-alkyl cross-couplings of unactivated secondary alkyl electrophiles: stereoconvergent Suzuki reactions of racemic acylated halohydrins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

6 September 2017

Asymmetric Suzuki cross-couplings of activated secondary alkyl electrophiles: arylations of racemic alpha-chloroamides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

6 September 2017

Chemoselectivity and the curious reactivity preferences of functional groups

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

6 September 2017

Highly regio- and enantioselective copper-catalyzed hydroboration of styrenes

1 reference

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6 September 2017

Homologation and alkylation of boronic esters and boranes by 1,2-metallate rearrangement of boronate complexes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

6 September 2017

Asymmetric hydroboration of 1,1-disubstituted alkenes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

6 September 2017

Simple, efficient, and modular syntheses of polyene natural products via iterative cross-coupling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

6 September 2017

Readily Available Unprotected Amino Aldehydes

1 reference

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6 September 2017

Efficient cross-coupling of secondary alkyltrifluoroborates with aryl chlorides--reaction discovery using parallel microscale experimentation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

27 September 2017

Iterative Cross-Couplng with MIDA Boronates: Towards a General Platform for Small Molecule Synthesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

23 June 2018

Stereospecific Cross-Coupling of Secondary Alkyl β-Trifluoroboratoamides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

23 June 2018

Gold-catalyzed oxidative coupling reactions with aryltrimethylsilanes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

23 June 2018

A simple and general platform for generating stereochemically complex polyene frameworks by iterative cross-coupling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

23 June 2018

Stereospecific Suzuki−Miyaura Coupling of Chiral α-(Acylamino)benzylboronic Esters with Inversion of Configuration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

23 June 2018

Enantioselective Synthesis of Boron-Substituted Quaternary Carbons by NHC−Cu-Catalyzed Boronate Conjugate Additions to Unsaturated Carboxylic Esters, Ketones, or Thioesters

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

23 June 2018

Stereoretentive Suzuki-Miyaura coupling of haloallenes enables fully stereocontrolled access to (-)-peridinin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

23 June 2018

Pt-catalyzed enantioselective diboration of terminal alkenes with B2(pin)2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

23 June 2018

Palladium-catalyzed enantioselective diboration of prochiral allenes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

23 June 2018

(Z)-(2-bromovinyl)-MIDA boronate: a readily accessible and highly versatile building block for small molecule synthesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

31 August 2018

Synthesis of 2-keto-anti-1,3-diols by chemoselective tandem oxidation of 2-B(pin)-substituted allylic alcohols.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

31 August 2018

General method for synthesis of 2-heterocyclic N-methyliminodiacetic acid boronates.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

31 August 2018

Asymmetric Rh(I)-catalyzed addition of MIDA boronates to N-tert-butanesulfinyl aldimines: development and comparison to trifluoroborates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

31 August 2018

Chiral boronate derivatives via catalytic enantioselective conjugate addition of Grignard reagents on 3-boronyl unsaturated esters and thioesters

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

31 August 2018

Amphoteric amino aldehydes reroute the aza-Michael reaction.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

31 August 2018

A general solution for unstable boronic acids: slow-release cross-coupling from air-stable MIDA boronates.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

31 August 2018

Cross coupling reactions of chiral secondary organoboronic esters with retention of configuration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

31 August 2018

Multistep synthesis of complex boronic acids from simple MIDA boronates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

31 August 2018

9-Borabicyclo[3.3.2]decanes and the asymmetric hydroboration of 1,1-disubstituted alkenes

1 reference

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31 August 2018

Enantioselective alkyl-alkyl Suzuki cross-couplings of unactivated homobenzylic halides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164213

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Expanding organoboron chemistry: epoxidation of potassium organotrifluoroborates

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Regio- and enantiocontrol in the room-temperature hydroboration of vinyl arenes with pinacol borane

1 reference

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31 August 2018

[3,3] Sigmatropic rearrangement of boron-containing allyl alcohols: synthesis of allyl addition reagents

1 reference

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31 August 2018

A Simple and Modular Strategy for Small Molecule Synthesis: Iterative Suzuki−Miyaura Coupling of B-Protected Haloboronic Acid Building Blocks

1 reference

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Synthesis and properties of MIDA boronate containing aromatic amino acids: new peptide building blocks

1 reference

https://pubmed.ncbi.nlm.nih.gov/21823591

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1 reference

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inferred from PubMed ID database lookup

Synthesis of Enantiomerically Pure Cyclopropanes from Cyclopropylboronic Acids†

1 reference

https://pubmed.ncbi.nlm.nih.gov/21823591

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inferred from PubMed ID database lookup

Catalytic asymmetric synthesis of chiral tertiary organoboronic esters through conjugate boration of beta-substituted cyclic enones

1 reference

https://pubmed.ncbi.nlm.nih.gov/21823591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Full chirality transfer in the conversion of secondary alcohols into tertiary boronic esters and alcohols using lithiation-borylation reactions

1 reference

https://pubmed.ncbi.nlm.nih.gov/21823591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epimerization- and protecting-group-free synthesis of peptidomimetic conjugates from amphoteric amino aldehydes

1 reference

https://pubmed.ncbi.nlm.nih.gov/21823591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Highly efficient Cu(I)-catalyzed synthesis of N-heterocycles through a cyclization-triggered addition of alkynes

1 reference

https://pubmed.ncbi.nlm.nih.gov/21823591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expanding the scope of transformations of organoboron species: carbon-carbon bond formation with retention of configuration

1 reference

https://pubmed.ncbi.nlm.nih.gov/21823591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Macrocyclization of linear peptides enabled by amphoteric molecules

1 reference

https://pubmed.ncbi.nlm.nih.gov/21823591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Total synthesis of (-)-aurantioclavine

1 reference

https://pubmed.ncbi.nlm.nih.gov/21823591

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1021/JA205912Y

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

1 September 2017

ResearchGate publication ID

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