(Q42112864)

English

Gold-catalyzed highly regioselective oxidation of C-C triple bonds without acid additives: propargyl moieties as masked α,β-unsaturated carbonyls.

scientific article published on October 2010

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14 February 2020

Gold-catalyzed highly regioselective oxidation of C-C triple bonds without acid additives: propargyl moieties as masked α,β-unsaturated carbonyls (English)

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14 February 2020

3

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14 February 2020

author name string

Biao Lu

1

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14 February 2020

Chaoqun Li

2

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14 February 2020

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publication date

1 October 2010

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14 February 2020

Journal of the American Chemical Society

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14 February 2020

132

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14 February 2020

40

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14 February 2020

14070-14072

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14 February 2020

Gold-catalyzed one-step practical synthesis of oxetan-3-ones from readily available propargylic alcohols.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978523

29 May 2018

Gold-catalyzed efficient synthesis of azepan-4-ones via a two-step [5 + 2] annulation.

1 reference

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29 May 2018

A general strategy for regiocontrol in nickel-catalyzed reductive couplings of aldehydes and alkynes

1 reference

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29 May 2018

Efficient synthesis of E-alpha-haloenones through chemoselective alkyne activation over allene with triazole-Au catalysts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978523

17 August 2018

Construction of 2,3-dihydrofuran cores through the [3+2] cycloaddition of gold alpha-carbonylcarbenoids with alkenes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978523

17 August 2018

Alkynes as equivalents of alpha-diazo ketones in generating alpha-oxo metal carbenes: a gold-catalyzed expedient synthesis of dihydrofuran-3-ones

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978523

17 August 2018

Geometry-dependent divergence in the gold-catalyzed redox cascade cyclization of o-alkynylaryl ketoximes and nitrones leading to isoindoles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978523

17 August 2018

A two-step, formal [4 + 2] approach toward piperidin-4-ones via Au catalysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978523

17 August 2018

Gold-catalyzed intramolecular redox reaction of sulfinyl alkynes: efficient generation of alpha-oxo gold carbenoids and application in insertion into R--CO bonds.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978523

17 August 2018

Rearrangement of alkynyl sulfoxides catalyzed by gold(I) complexes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2978523

17 August 2018

A Convenient Method for the Preparation of (Z)-alpha,beta-Unsaturated Carbonyl Compounds

1 reference

https://pubmed.ncbi.nlm.nih.gov/20853846

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reactive intermediates from DMDO oxidation of ynamides. Trapping of a de novo chiral push-pull carbene via cyclopropanation

1 reference

https://pubmed.ncbi.nlm.nih.gov/20853846

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gold-catalyzed efficient preparation of linear alpha-iodoenones from propargylic acetates

1 reference

https://pubmed.ncbi.nlm.nih.gov/20853846

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gold or no gold: one-pot synthesis of tetrahydrobenz[b]azepin-4-ones from tertiary N-(but-3-ynyl)anilines

1 reference

https://pubmed.ncbi.nlm.nih.gov/20853846

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Olefination of ketones using a gold(III)-catalyzed Meyer-Schuster rearrangement

1 reference

https://pubmed.ncbi.nlm.nih.gov/20853846

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gold-catalyzed waste-free generation and reaction of azomethine ylides: internal redox/dipolar cycloaddition cascade

1 reference

https://pubmed.ncbi.nlm.nih.gov/20853846

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Stereoselective one-pot synthesis of 1-aminoindanes and 5,6-fused azacycles using a gold-catalyzed redox-pinacol-Mannich-Michael cascade

1 reference

https://pubmed.ncbi.nlm.nih.gov/20853846

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dioxygen activation under ambient conditions: Cu-catalyzed oxidative amidation-diketonization of terminal alkynes leading to alpha-ketoamides

1 reference

https://pubmed.ncbi.nlm.nih.gov/20853846

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Practical synthesis of linear alpha-iodo/bromo-alpha,beta-unsaturated aldehydes/ketones from propargylic alcohols via Au/Mo bimetallic catalysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/20853846

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gold catalysis: switching the pathway of the furan-yne cyclization

1 reference

https://pubmed.ncbi.nlm.nih.gov/20853846

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Wacker-type oxidation of alkynes into 1,2-diketones using molecular oxygen

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diversity in gold- and silver-catalyzed cycloisomerization of epoxide-alkyne functionalities

1 reference

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12 December 2020

based on heuristic

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[(NHC)AuI]-Catalyzed Formation of Conjugated Enones and Enals: An Experimental and Computational Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/20853846

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gold- or platinum-catalyzed synthesis of sulfur heterocycles: access to sulfur ylides without using sacrificial functionality

1 reference

https://pubmed.ncbi.nlm.nih.gov/20853846

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1021/JA1072614

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20853846%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20853846%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20853846%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

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