Thiourea-catalyzed enantioselective cyanosilylation of ketones (Q38304709)

1 September 2017

Thiourea-catalyzed enantioselective cyanosilylation of ketones (English)

1 reference

1 September 2017

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Douglas E Fuerst

1

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PMC publication ID

3166885

1 September 2017

Eric N Jacobsen

series ordinal

2

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PMC publication ID

3166885

1 September 2017

language of work or name

English

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publication date

1 June 2005

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Journal of the American Chemical Society

1 September 2017

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1 September 2017

127

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1 September 2017

25

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1 September 2017

8964-8965

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Highly enantioselective conjugate addition of nitromethane to chalcones using bifunctional cinchona organocatalysts.

1 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166885

Activation of carbonyl compounds by double hydrogen bonding: an emerging tool in asymmetric catalysis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166885

Enantioselective Michael Reaction of Malonates to Nitroolefins Catalyzed by Bifunctional Organocatalysts

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166885

Asymmetric Morita−Baylis−Hillman Reactions Catalyzed by Chiral Brønsted Acids

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166885

Metal-free organocatalysis through explicit hydrogen bonding interactions

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166885

Catalytic asymmetric cyanosilylation of ketones with chiral Lewis base

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166885

Hydrogen bonding: single enantiomers from a chiral-alcohol catalyst.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166885

Metal-free, noncovalent catalysis of diels-alder reactions by neutral hydrogen bond donors in organic solvents and in water

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166885

H-bonding additives act like Lewis acid catalysts

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166885

Hydrogen bonds and proton transfer in general-catalytic transition-state stabilization in enzyme catalysis.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166885

A General Catalyst for the Asymmetric Strecker Reaction This work was supported by the NIH (GM-43214). A postdoctoral fellowship to M.S.S. (NIH), and a predoctoral fellowship to P.V. sponsored by Alfred Bader are gratefully acknowledged

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166885

Hydrogen bonding in enzymatic catalysis: analysis of energetic contributions

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166885

Enantioselective cyanosilylation of ketones catalyzed by a chiral oxazaborolidinium ion.

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166885

Second-generation organocatalysts for the highly enantioselective dynamic kinetic resolution of azlactones

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166885

Highly efficient dynamic kinetic resolution of azlactones by urea-based bifunctional organocatalysts

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166885

Highly enantioselective thiourea-catalyzed nitro-Mannich reactions

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166885

Highly enantioselective catalytic acyl-pictet-spengler reactions

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166885

Thiourea-catalyzed enantioselective hydrophosphonylation of imines: practical access to enantiomerically enriched alpha-amino phosphonic acids

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166885

Aluminum-catalyzed asymmetric addition of TMSCN to aromatic and aliphatic ketones promoted by an easily accessible and recyclable peptide ligand

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166885

Asymmetric catalytic Mannich reactions catalyzed by urea derivatives: enantioselective synthesis of beta-aryl-beta-amino acids

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166885

Structure-based analysis and optimization of a highly enantioselective catalyst for the strecker reaction

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166885

Switching enantiofacial selectivities using one chiral source: catalytic enantioselective synthesis of the key intermediate for (20S)-camptothecin family by (S)-selective cyanosilylation of ketones

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166885

A highly enantioselective chiral Lewis base-catalyzed asymmetric cyanation of ketones

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3166885

Enantioselective aza-Henry reaction catalyzed by a bifunctional organocatalyst

31 August 2018

1 reference

12 December 2020

Enantioselective catalytic addition of HCN to ketoimines. Catalytic synthesis of quaternary amino acids

1 reference

12 December 2020

Enantioselective cyanosilylation of ketones by a catalytic double-activation method employing chiral Lewis acid and achiral N-oxide catalysts

1 reference

12 December 2020

Chemically catalyzed asymmetric cyanohydrin syntheses

1 reference

12 December 2020

Cyanohydrins in Nature and the Laboratory: Biology, Preparations, and Synthetic Applications

1 reference

12 December 2020

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Identifiers

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30 July 2022

release_7ca62tbibree3h4k3znlumcyeq

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/7ca62tbibree3h4k3znlumcyeq

30 July 2022

https://api.fatcat.wiki/v0/release/7ca62tbibree3h4k3znlumcyeq

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30 July 2022

https://api.fatcat.wiki/v0/release/7ca62tbibree3h4k3znlumcyeq

PubMed publication ID

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30 July 2022