(Q35808518)

English

Formation of C-C Bonds via Catalytic Hydrogenation and Transfer Hydrogenation: Vinylation, Allylation, and Enolate Addition of Carbonyl Compounds and Imines

scientific article published on January 2008

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Europe PubMed Central

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25 January 2020

Formation of C-C Bonds via Catalytic Hydrogenation and Transfer Hydrogenation: Vinylation, Allylation, and Enolate Addition of Carbonyl Compounds and Imines (English)

1 reference

Europe PubMed Central

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25 January 2020

Michael J. Krische

4

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Michael J Krische

1 reference

Europe PubMed Central

10 August 2017

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Ryan L Patman

1

1 reference

Europe PubMed Central

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25 January 2020

John F Bower

2

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25 January 2020

In Su Kim

3

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Europe PubMed Central

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25 January 2020

Michael J Krische

4

1 reference

Europe PubMed Central

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25 January 2020

publication date

1 January 2008

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25 January 2020

Aldrichimica Acta

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25 January 2020

41

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25 January 2020

4

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25 January 2020

95-104

1 reference

Europe PubMed Central

PMC publication ID

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25 January 2020

Carbonyl propargylation from the alcohol or aldehyde oxidation level employing 1,3-enynes as surrogates to preformed allenylmetal reagents: a ruthenium-catalyzed C-C bond-forming transfer hydrogenation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

27 July 2018

Ruthenium-catalyzed C-C bond forming transfer hydrogenation: carbonyl allylation from the alcohol or aldehyde oxidation level employing acyclic 1,3-dienes as surrogates to preformed allyl metal reagents

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

27 July 2018

Enantioselective iridium-catalyzed carbonyl allylation from the alcohol or aldehyde oxidation level using allyl acetate as an allyl metal surrogate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

27 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

27 July 2018

Iridium-catalyzed C-C coupling via transfer hydrogenation: carbonyl addition from the alcohol or aldehyde oxidation level employing 1,3-cyclohexadiene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

27 July 2018

Catalytic asymmetric generation of (Z)-disubstituted allylic alcohols

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

27 July 2018

Catalytic C-C coupling via transfer hydrogenation: reverse prenylation, crotylation, and allylation from the alcohol or aldehyde oxidation level

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

27 July 2018

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=3295582

27 July 2018

High-throughput and parallel screening methods in asymmetric hydrogenation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

27 July 2018

Hydrogen-mediated reductive coupling of conjugated alkynes with ethyl (N-Sulfinyl)iminoacetates: synthesis of unnatural alpha-amino acids via rhodium-catalyzed C-C bond forming hydrogenation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

27 July 2018

Enamine-based organocatalysis with proline and diamines: the development of direct catalytic asymmetric Aldol, Mannich, Michael, and Diels-alder reactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

27 July 2018

Recent advances in the activation of boron and silicon reagents for stereocontrolled allylation reactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

27 July 2018

A general, highly enantioselective method for the synthesis of D and L alpha-amino acids and allylic amines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

27 July 2018

Novel applications of alkenyl zirconocenes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

27 July 2018

Stereoselective synthesis of stereotriad subunits of polyketides through additions of nonracemic allenylsilanes to (R)- and (S)-2-methyl-3-oxygenated propanals

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

27 July 2018

The atom economy--a search for synthetic efficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

27 July 2018

Ruthenium catalyzed C-C bond formation via transfer hydrogenation: branch-selective reductive coupling of allenes to paraformaldehyde and higher aldehydes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 2018

Cobalt-catalyzed reductive Mannich reactions of 4-acryloylmorpholine with N-tosyl aldimines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 2018

Enantioselective iridium-catalyzed imine vinylation: optically enriched allylic amines via alkyne-imine reductive coupling mediated by hydrogen

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 2018

Carbonyl allylation in the absence of preformed allyl metal reagents: reverse prenylation via iridium-catalyzed hydrogenative coupling of dimethylallene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 2018

Chiral allylic and allenic metal reagents for organic synthesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 2018

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=3295582

25 September 2018

Enantioselective reductive coupling of 1,3-enynes to heterocyclic aromatic aldehydes and ketones via rhodium-catalyzed asymmetric hydrogenation: mechanistic insight into the role of Brønsted acid additives.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 2018

Catalytic carbonyl Z-dienylation via multicomponent reductive coupling of acetylene to aldehydes and alpha-ketoesters mediated by hydrogen: Carbonyl insertion into cationic rhodacyclopentadienes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 2018

Highly enantioselective reductive cyclization of acetylenic aldehydes via rhodium catalyzed asymmetric hydrogenation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 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=3295582

25 September 2018

Highly enantioselective direct reductive coupling of conjugated alkynes and alpha-ketoesters via rhodium-catalyzed asymmetric hydrogenation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 2018

Access to macrocyclic endocyclic and exocyclic allylic alcohols by nickel-catalyzed reductive cyclization of ynals

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 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=3295582

25 September 2018

Catalytic asymmetric vinylation and dienylation of ketones

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 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=3295582

25 September 2018

Catalytic asymmetric addition of alkylzinc and functionalized alkylzinc reagents to ketones.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 2018

Asymmetric allylic alkylation, an enabling methodology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 2018

Asymmetric catalytic coupling of organoboranes, alkynes, and imines with a removable (trialkylsilyloxy)ethyl group--direct access to enantiomerically pure primary allylic amines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 2018

Catalytic asymmetric vinylation of ketones

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 2018

Ligand-dependent scope and divergent mechanistic behavior in nickel-catalyzed reductive couplings of aldehydes and alkynes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 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=3295582

25 September 2018

Enantioselective catalytic allylation of carbonyl groups by umpolung of pi-allyl palladium complexes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 2018

Current progress in the asymmetric aldol addition reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 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=3295582

25 September 2018

Catalytic Enantioselective Addition of Allylic Organometallic Reagents to Aldehydes and Ketones

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 2018

Pd-catalyzed nucleophilic alkylation of aliphatic aldehydes with allyl alcohols: allyl, 2-tetrahydrofuryl, and 2-tetrahydropyranyl ethers as useful C3, C4, and C5 sources

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 2018

Catalytic asymmetric reductive coupling of alkynes and aldehydes: enantioselective synthesis of allylic alcohols and alpha-hydroxy ketones

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 2018

A convenient, one-step synthesis of optically active tertiary aminonaphthol and its applications in the highly enantioselective alkenylations of aldehydes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 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=3295582

25 September 2018

Rhodium-catalyzed approach to Mannich-type products using aldimine, alpha,beta-unsaturated ester, and hydrosilane.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 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=3295582

25 September 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=3295582

25 September 2018

Asymmetric Aldol reaction via a dinuclear zinc catalyst: alpha-hydroxyketones as donors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 2018

Direct catalytic asymmetric aldol reaction: synthesis of either syn- or anti-alpha,beta-dihydroxy ketones.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 2018

The Catalytic Asymmetric Aldol Reaction.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3295582

25 September 2018

Strained silacycles in organic synthesis: a new reagent for the enantioselective allylation of aldehydes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[2,2]paracyclophane-based N,O-ligands in alkenylzinc additions to aldehydes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enantioselective reductive coupling of 1,3-enynes to glyoxalates mediated by hydrogen: asymmetric synthesis of beta,gamma-unsaturated alpha-hydroxy esters

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Highly selective catalytic intermolecular reductive coupling of alkynes and aldehydes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catalytic asymmetric synthesis of macrocyclic (E)-allylic alcohols from omega-alkynals via intramolecular 1-alkenylzinc/aldehyde additions

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

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/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rhodium-catalyzed reductive mannich coupling of vinyl ketones to N-sulfonylimines mediated by hydrogen

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alpha-hydroxy esters via enantioselective hydrogen-mediated C-C coupling: regiocontrolled reactions of silyl-substituted 1,3-diynes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catalytic asymmetric synthesis of hydroxy enol ethers: approach to a two-carbon homologation of aldehydes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

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/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Asymmetric transition-metal-catalyzed allylic alkylations: applications in total synthesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

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/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A catalytic asymmetric method for the synthesis of gamma-unsaturated beta-amino acid derivatives

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

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/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Highly enantioselective synthesis of (E)-allylic alcohols

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Creation of quaternary stereocenters in carbonyl allylation reactions

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lewis base activation of Lewis acids: catalytic enantioselective allylation and propargylation of aldehydes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allylic Amination

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Highly regioselective, catalytic asymmetric reductive coupling of 1,3-enynes and ketones

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alcohols as electrophiles in C--C bond-forming reactions: the hydrogen autotransfer process

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

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/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allylic amines via iridium-catalyzed C-C bond forming hydrogenation: imine vinylation in the absence of stoichiometric byproducts or metallic reagents

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dimethylzinc-mediated additions of alkenylzirconocenes to aldimines. New methodologies for allylic amine and C-cyclopropylalkylamine syntheses

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Acyclic stereocontrol through the aldol condensation

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catalytic, enantioselective addition of substituted allylic trichlorosilanes using a rationally-designed 2,2'-bispyrrolidine-based bisphosphoramide

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

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/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Solid-phase synthesis of chiral N-acylethylenediamines and their use as ligands for the asymmetric addition of alkylzinc and alkenylzinc reagents to aldehydes

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Direct, stereospecific generation of (Z)-disubstituted allylic alcohols

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

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/22403445

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/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enantioselective reductive coupling of acetylene to N-arylsulfonyl imines via rhodium catalyzed C-C bond-forming hydrogenation: (Z)-dienyl allylic amines

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Stereoselective synthesis of trans beta-lactams through iridium-catalyzed reductive coupling of imines and acrylates

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

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/22403445

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/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chiral Allylic and Allenic Stannanes as Reagents for Asymmetric Synthesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

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/22403445

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/22403445

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/22403445

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/22403445

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/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regioselective reductive coupling of alkynes and aldehydes leading to allylic alcohols

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enantiomerically enriched allylic alcohols and allylic amines via C-C bond-forming hydrogenation: asymmetric carbonyl and imine vinylation

1 reference

https://pubmed.ncbi.nlm.nih.gov/22403445

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/22403445

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22403445%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22403445%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

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