(Q40233411)

English

Diastereo- and enantioselective hydrogenative aldol coupling of vinyl ketones: design of effective monodentate TADDOL-like phosphonite ligands

scientific article published on 12 February 2008

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scholarly article

1 reference

Europe PubMed Central

18 September 2017

Diastereo- and enantioselective hydrogenative aldol coupling of vinyl ketones: design of effective monodentate TADDOL-like phosphonite ligands (English)

1 reference

Europe PubMed Central

18 September 2017

enantioselectivity

1 reference

based on heuristic

inferred from title

Michael J. Krische

5

object named as

Michael J Krische

1 reference

Europe PubMed Central

18 September 2017

author name string

Cisco Bee

1

1 reference

Europe PubMed Central

18 September 2017

Soo Bong Han

2

1 reference

Europe PubMed Central

18 September 2017

Abbas Hassan

3

1 reference

Europe PubMed Central

18 September 2017

Hiroki Iida

4

1 reference

Europe PubMed Central

18 September 2017

language of work or name

0 references

publication date

12 February 2008

1 reference

Europe PubMed Central

18 September 2017

Journal of the American Chemical Society

1 reference

Europe PubMed Central

18 September 2017

130

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Europe PubMed Central

18 September 2017

2746-2747

1 reference

Europe PubMed Central

18 September 2017

9

1 reference

Europe PubMed Central

18 September 2017

A three-component tandem reductive aldol reaction catalyzed by N-heterocyclic carbene-copper complexes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860773

22 September 2017

Intermolecular asymmetric reductive aldol reaction of ketones as acceptors promoted by chiral Rh(Phebox) catalyst.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860773

20 August 2018

Highly diastereo- and enantioselective copper-catalyzed domino reduction/aldol reaction of ketones with methyl acrylate.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860773

20 August 2018

Cu(I)-catalyzed reductive aldol cyclizations: diastereo- and enantioselective synthesis of beta-hydroxylactones.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860773

20 August 2018

A highly efficient organocatalyst for direct aldol reactions of ketones with aldehydes [corrected].

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860773

20 August 2018

High performance of Rh(Phebox) catalysts in asymmetric reductive aldol reaction: high anti-selectivity.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860773

20 August 2018

Metallo-aldehyde enolates via enal hydrogenation: catalytic cross aldolization with glyoxal partners as applied to the synthesis of 3,5-disubstituted pyridazines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860773

20 August 2018

Catalytic generation of indium hydride in a highly diastereoselective reductive aldol reaction.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860773

20 August 2018

Diastereoselective cycloreductions and cycloadditions catalyzed by Co(dpm)(2)-silane (dpm = 2,2,6,6-tetramethylheptane-3,5-dionate): mechanism and partitioning of hydrometallative versus anion radical pathways

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860773

20 August 2018

2-furyl phosphines as ligands for transition-metal-mediated organic synthesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860773

20 August 2018

Amino acid catalyzed direct asymmetric aldol reactions: a bioorganic approach to catalytic asymmetric carbon-carbon bond-forming reactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860773

20 August 2018

Diastereoselective cobalt-catalyzed aldol and Michael cycloreductions.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2860773

20 August 2018

Hydrogen-mediated aldol reductive coupling of vinyl ketones catalyzed by rhodium: high syn-selectivity through the effect of tri-2-furylphosphine

1 reference

https://pubmed.ncbi.nlm.nih.gov/18266373

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hydrogen-Mediated C−C Bond Formation: A Broad New Concept in Catalytic C−C Coupling1

1 reference

https://pubmed.ncbi.nlm.nih.gov/18266373

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple primary-tertiary diamine-Brønsted acid catalyst for asymmetric direct aldol reactions of linear aliphatic ketones

1 reference

https://pubmed.ncbi.nlm.nih.gov/18266373

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diastereoselective Intermolecular Cobalt-Catalyzed Reductive Aldol Reactions of α,β-Unsaturated Amides with Ketones

1 reference

https://pubmed.ncbi.nlm.nih.gov/18266373

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reductive generation of enolates from enones using elemental hydrogen: catalytic C-C bond formation under hydrogenative conditions

1 reference

https://pubmed.ncbi.nlm.nih.gov/18266373

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dramatic ligand effect in catalytic asymmetric reductive aldol reaction of allenic esters to ketones

1 reference

https://pubmed.ncbi.nlm.nih.gov/18266373

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reductive aldol coupling of divinyl ketones via rhodium-catalyzed hydrogenation: syn-diastereoselective construction of beta-hydroxyenones

1 reference

https://pubmed.ncbi.nlm.nih.gov/18266373

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Asymmetric induction in hydrogen-mediated reductive aldol additions to alpha-amino aldehydes catalyzed by rhodium: selective formation of syn-stereotriads directed by intramolecular hydrogen-bonding

1 reference

https://pubmed.ncbi.nlm.nih.gov/18266373

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Surprising role of aryl halides in nickel-catalyzed reductive aldol reactions

1 reference

https://pubmed.ncbi.nlm.nih.gov/18266373

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diastereoselective Synthesis of 4-Hydroxypiperidin-2-ones via Cu(I)-Catalyzed Reductive Aldol Cyclization†

1 reference

https://pubmed.ncbi.nlm.nih.gov/18266373

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enantio- and diastereoselective reductive aldol reactions with iridium-pybox catalysts

1 reference

https://pubmed.ncbi.nlm.nih.gov/18266373

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Copper(I)-catalyzed enantio- and diastereoselective tandem reductive aldol reaction

1 reference

https://pubmed.ncbi.nlm.nih.gov/18266373

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Generation of (E)-silylketene acetals in a Rhodium-DuPhos catalyzed two-step reductive aldol reaction

1 reference

https://pubmed.ncbi.nlm.nih.gov/18266373

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rhodium-catalyzed reductive aldol reactions using aldehydes as the stoichiometric reductants

1 reference

https://pubmed.ncbi.nlm.nih.gov/18266373

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catalytic addition of metallo-aldehyde enolates to ketones: a new C-C bond-forming hydrogenation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18266373

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Stoichiometric and catalytic reductive aldol cyclizations of alkynediones induced by Stryker's reagent

1 reference

https://pubmed.ncbi.nlm.nih.gov/18266373

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enolate generation under hydrogenation conditions: catalytic aldol cycloreduction of keto-enones

1 reference

https://pubmed.ncbi.nlm.nih.gov/18266373

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diastereoselective Cobalt-Catalyzed Reductive Aldol Cyclizations Using Diethylzinc as the Stoichiometric Reductant

1 reference

https://pubmed.ncbi.nlm.nih.gov/18266373

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1021/JA710862U

1 reference

Europe PubMed Central

18 September 2017

release_nrmvoeue6zbzjoybstsxnpefpu

1 reference

https://api.fatcat.wiki/v0/release/nrmvoeue6zbzjoybstsxnpefpu

24 November 2022

based on heuristic

mapped directly with Wikidata item

1 reference

Europe PubMed Central

18 September 2017

1 reference

Europe PubMed Central

18 September 2017

ResearchGate publication ID

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