(Q41453616)

English

Stereoselective Syntheses of α,β-Unsaturated γ-Amino Esters Through Phosphine-Catalyzed γ-Umpolung Additions of Sulfonamides to γ-Substituted Allenoates

scientific article published on June 2015

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

30 September 2017

Stereoselective Syntheses of α,β-Unsaturated γ-Amino Esters Through Phosphine-Catalyzed γ-Umpolung Additions of Sulfonamides to γ-Substituted Allenoates (English)

1 reference

Europe PubMed Central

PMC publication ID

30 September 2017

stereoselectivity

1 reference

based on heuristic

inferred from title

3

object named as

Ohyun Kwon

1 reference

Europe PubMed Central

PMC publication ID

30 September 2017

author name string

Qing-Fa Zhou

1

1 reference

Europe PubMed Central

PMC publication ID

30 September 2017

Kui Zhang

2

1 reference

Europe PubMed Central

PMC publication ID

30 September 2017

publication date

1 June 2015

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Europe PubMed Central

PMC publication ID

30 September 2017

Tetrahedron Letters

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Europe PubMed Central

PMC publication ID

30 September 2017

56

1 reference

Europe PubMed Central

PMC publication ID

30 September 2017

23

1 reference

Europe PubMed Central

PMC publication ID

30 September 2017

3273-3276

1 reference

Europe PubMed Central

PMC publication ID

30 September 2017

Chiral phosphines in nucleophilic organocatalysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4450090

30 September 2017

Phosphine catalysis of allenes with electrophiles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4450090

30 September 2017

Advances in nucleophilic phosphine catalysis of alkenes, allenes, alkynes, and MBHADs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4450090

30 September 2017

Catalytic asymmetric C-N bond formation: phosphine-catalyzed intra- and intermolecular γ-addition of nitrogen nucleophiles to allenoates and alkynoates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4450090

30 September 2017

Enantioselective total synthesis of (+)-ibophyllidine via an asymmetric phosphine-catalyzed [3 + 2] annulation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4450090

30 September 2017

Enantioselective Carbon-Sulfur Bond Formation: γ Additions of Aryl Thiols to Allenoates Catalyzed by a Chiral Phosphepine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4450090

30 September 2017

Phosphine-initiated general base catalysis: facile access to benzannulated 1,3-diheteroatom five-membered rings via double-Michael reactions of allenes

1 reference

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Diversity through a branched reaction pathway: generation of multicyclic scaffolds and identification of antimigratory agents.

1 reference

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30 September 2017

Phosphine-catalyzed asymmetric additions of malonate esters to {gamma}-substituted allenoates and allenamides.

1 reference

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30 September 2017

Multifunctional chiral phosphine organocatalysts in catalytic asymmetric Morita-Baylis-Hillman and related reactions.

1 reference

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30 September 2017

Phosphine-catalyzed formation of carbon-sulfur bonds: catalytic asymmetric synthesis of gamma-thioesters

1 reference

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30 September 2017

Enantioselective catalysis and complexity generation from allenoates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4450090

30 September 2017

Asymmetric carbon-carbon bond formation gamma to a carbonyl group: phosphine-catalyzed addition of nitromethane to allenes

1 reference

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30 September 2017

Combinatorial strategies by marine cyanobacteria: symplostatin 4, an antimitotic natural dolastatin 10/15 hybrid that synergizes with the coproduced HDAC inhibitor largazole

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4450090

30 September 2017

Phosphine-catalyzed enantioselective synthesis of oxygen heterocycles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4450090

30 September 2017

Antimalarial peptides from marine cyanobacteria: isolation and structural elucidation of gallinamide A.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4450090

30 September 2017

Phosphine-triggered synthesis of functionalized cyclic compounds

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4450090

30 September 2017

Stable tetravalent phosphonium enolate zwitterions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4450090

30 September 2017

Design and synthesis of a novel class of furan-based molecules as potential 20S proteasome inhibitors.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4450090

30 September 2017

Syringolin A, a new plant elicitor from the phytopathogenic bacterium Pseudomonas syringae pv. syringae, inhibits the proliferation of neuroblastoma and ovarian cancer cells and induces apoptosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4450090

30 September 2017

Phosphine-catalyzed intramolecular γ-umpolung addition of α-aminoalkylallenic esters: facile synthesis of 3-carbethoxy-2-alkyl-3-pyrrolines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4450090

11 June 2018

Total synthesis, stereochemical assignment, and antimalarial activity of gallinamide A.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4450090

11 June 2018

Phosphine-catalyzed β'-umpolung addition of nucleophiles to activated α-alkyl allenes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4450090

11 June 2018

Phosphine-promoted [3 + 3] annulations of aziridines with allenoates: facile entry into highly functionalized tetrahydropyridines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4450090

11 June 2018

Bisphosphine-catalyzed mixed double-Michael reactions: asymmetric synthesis of oxazolidines, thiazolidines, and pyrrolidines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4450090

11 June 2018

Total synthesis of syringolin A.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4450090

19 August 2018

Phosphine-catalyzed synthesis of highly functionalized coumarins.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4450090

19 August 2018

Theoretical rationale for regioselection in phosphine-catalyzed allenoate additions to acrylates, imines, and aldehydes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4450090

19 August 2018

Miraziridine A: natures blueprint towards protease class-spanning inhibitors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4450090

19 August 2018

An Expedient Phosphine-Catalyzed [4 + 2] Annulation: Synthesis of Highly Functionalized Tetrahydropyridines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4450090

19 August 2018

A total synthesis of (-)-hemiasterlin using N-Bts methodology

1 reference

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19 August 2018

Reactions of electron-deficient alkynes and allenes under phosphine catalysis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4450090

19 August 2018

Synthesis of gamma,delta-didehydrohomoglutamates by the phosphine-catalyzed gamma-addition reaction to acetylenic esters

1 reference

https://pubmed.ncbi.nlm.nih.gov/26041942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Development of asymmetric phosphine-promoted annulations of allenes with electron-deficient olefins and imines

1 reference

https://pubmed.ncbi.nlm.nih.gov/26041942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Total synthesis and antimalarial activity of symplostatin 4

1 reference

https://pubmed.ncbi.nlm.nih.gov/26041942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cytotoxic peptides hemiasterlin, hemiasterlin A and hemiasterlin B induce mitotic arrest and abnormal spindle formation

1 reference

https://pubmed.ncbi.nlm.nih.gov/26041942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Engaging zwitterions in carbon-carbon and carbon-nitrogen bond-forming reactions: A promising synthetic strategy

1 reference

https://pubmed.ncbi.nlm.nih.gov/26041942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Stereoselective syntheses of functionalized spirocyclopenteneoxindoles via triphenylphosphine-catalyzed [3+2] cycloaddition reactions

1 reference

https://pubmed.ncbi.nlm.nih.gov/26041942

12 December 2020

based on heuristic

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Enantioselective Organocatalytic Conjugate Reduction of β-Azole-Containing α,β-Unsaturated Aldehydes

1 reference

https://pubmed.ncbi.nlm.nih.gov/26041942

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based on heuristic

inferred from PubMed ID database lookup

Synthesis and antimitotic/cytotoxic activity of hemiasterlin analogues

1 reference

https://pubmed.ncbi.nlm.nih.gov/26041942

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.TETLET.2015.01.120

1 reference

Europe PubMed Central

PMC publication ID

30 September 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

30 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

30 September 2017

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