(Q41814011)

English

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

scientific article published on August 2005

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

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 (English)

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

Michael J. Krische

3

object named as

Michael J Krische

1 reference

Europe PubMed Central

12 October 2017

PMC publication ID

author name string

Jong-Rock Kong

1

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

Chang-Woo Cho

2

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

language of work or name

0 references

publication date

1 August 2005

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

number of pages

8

1 reference

based on heuristic

inferred from page(s)

Journal of the American Chemical Society

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

127

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

32

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

11269-11276

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

Catalytic C-C bond formation via capture of hydrogenation intermediates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2625294

6 June 2018

Nickel-catalyzed reductive cyclizations and couplings.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2625294

6 June 2018

Alpha-imino esters: versatile substrates for the catalytic, asymmetric synthesis of alpha- and beta-amino acids and beta-lactams

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2625294

6 June 2018

N-tert-Butanesulfinyl Imines: Versatile Intermediates for the Asymmetric Synthesis of Amines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2625294

6 June 2018

Synthesis of organotitanium complexes from alkenes and alkynes and their synthetic applications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2625294

6 June 2018

Rhodium boryl complexes in the catalytic, terminal functionalization of alkanes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2625294

18 August 2018

Chemoselective construction of substituted conjugated dienes using an olefin cross-metathesis protocol.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2625294

18 August 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=2625294

18 August 2018

Catalytic enantioselective synthesis of sulfinate esters through the dynamic resolution of tert-butanesulfinyl chloride

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2625294

18 August 2018

Hydrogen-mediated C-C bond formation: catalytic regio- and stereoselective reductive condensation of alpha-keto aldehydes and 1,3-enynes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2625294

18 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=2625294

18 August 2018

Iridium-mediated asymmetric hydrogenation of 2,3-diphenylbutadiene: a revealing kinetic study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2625294

18 August 2018

First catalytic reductive coupling of 1,3-diynes to carbonyl partners: a new regio- and enantioselective 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=2625294

18 August 2018

Catalytic three-component coupling of alkynes, imines, and organoboron reagents

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2625294

18 August 2018

Properly designed modular asymmetric synthesis for enantiopure sulfinamide auxiliaries from N-sulfonyl-1,2,3-oxathiazolidine-2-oxide agents

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2625294

18 August 2018

A New catalytic C[bond]C bond-forming hydrogenation: reductive coupling of dienes and glyoxals under catalytic hydrogenation conditions

1 reference

https://pubmed.ncbi.nlm.nih.gov/16089454

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/16089454

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alkene-directed, nickel-catalyzed alkyne coupling reactions

1 reference

https://pubmed.ncbi.nlm.nih.gov/16089454

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enantioselective total synthesis of (+)-testudinariol a using a new nickel-catalyzed allenyl aldehyde cyclization

1 reference

https://pubmed.ncbi.nlm.nih.gov/16089454

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nickel-catalyzed cyclizations, couplings, and cycloadditions involving three reactive components

1 reference

https://pubmed.ncbi.nlm.nih.gov/16089454

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rhodium-catalyzed reductive cyclization of 1,6-diynes and 1,6-enynes mediated by hydrogen: catalytic C-C bond formation via capture of hydrogenation intermediates

1 reference

https://pubmed.ncbi.nlm.nih.gov/16089454

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Asymmetric synthesis of alpha-amino 1,3-dithioketals from sulfinimines (N-sulfinyl imines). Synthesis of (2S,3R)-(-)-3-hydroxy-3-methylproline

1 reference

https://pubmed.ncbi.nlm.nih.gov/16089454

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Preparation of homoallylic alcohols by nickel-catalyzed cyclizations of allenyl aldehydes

1 reference

https://pubmed.ncbi.nlm.nih.gov/16089454

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enantioselective reductive cyclization of 1,6-enynes via rhodium-catalyzed asymmetric hydrogenation: C-C bond formation precedes hydrogen activation

1 reference

https://pubmed.ncbi.nlm.nih.gov/16089454

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nickel‐Catalyzed Coupling of Carbonyl Compounds and Alkynes or 1,3‐Dienes: An Efficient Method for the Preparation of Allylic, Homoallylic, and Bishomoallylic Alcohols

1 reference

https://pubmed.ncbi.nlm.nih.gov/16089454

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/16089454

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/16089454

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1021/JA051104I

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

release_vk7chfzyfbhwbibdbnxco4jwhq

1 reference

https://api.fatcat.wiki/v0/release/vk7chfzyfbhwbibdbnxco4jwhq

24 November 2022

based on heuristic

mapped directly with Wikidata item

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

ResearchGate publication ID

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