(Q34144693)

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Total synthesis of (+)-roxaticin via C-C bond forming transfer hydrogenation: a departure from stoichiometric chiral reagents, auxiliaries, and premetalated nucleophiles in polyketide construction

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scholarly article

1 reference

Europe PubMed Central

31 July 2017

Total synthesis of (+)-roxaticin via C-C bond forming transfer hydrogenation: a departure from stoichiometric chiral reagents, auxiliaries, and premetalated nucleophiles in polyketide construction (English)

1 reference

Europe PubMed Central

31 July 2017

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Michael J. Krische

4

object named as

Michael J Krische

1 reference

Europe PubMed Central

31 July 2017

author name string

Soo Bong Han

1

1 reference

Europe PubMed Central

31 July 2017

Abbas Hassan

2

1 reference

Europe PubMed Central

31 July 2017

In Su Kim

3

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Europe PubMed Central

31 July 2017

language of work or name

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publication date

1 November 2010

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Europe PubMed Central

31 July 2017

Journal of the American Chemical Society

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Europe PubMed Central

31 July 2017

132

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Europe PubMed Central

31 July 2017

15559-15561

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Europe PubMed Central

31 July 2017

44

1 reference

Europe PubMed Central

31 July 2017

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

1 reference

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Formation of C-C Bonds via Ruthenium Catalyzed Transfer Hydrogenation: Carbonyl Addition from the Alcohol or Aldehyde Oxidation Level

1 reference

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Iridium Catalyzed Hydro-hydroxyalkylation of Butadiene: Carbonyl Crotylation

1 reference

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Iridium-catalyzed anti-diastereo- and enantioselective carbonyl (trimethylsilyl)allylation from the alcohol or aldehyde oxidation level

1 reference

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anti-Diastereo- and enantioselective carbonyl (hydroxymethyl)allylation from the alcohol or aldehyde oxidation level: allyl carbonates as allylmetal surrogates

1 reference

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5 July 2018

De Novo Asymmetric Syntheses of (+)-Goniothalamin, (+)-Goniothalamin oxide and 7,8-Bis-epi-Goniothalamin using Asymmetric Allylations

1 reference

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Diastereo- and enantioselective anti-alkoxyallylation employing allylic gem-dicarboxylates as allyl donors via iridium-catalyzed transfer hydrogenation

1 reference

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Enantioselective iridium-catalyzed carbonyl allylation from the alcohol oxidation level via transfer hydrogenation: minimizing pre-activation for synthetic efficiency

1 reference

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Enantioselective allylation, crotylation, and reverse prenylation of substituted isatins: iridium-catalyzed C-C bond-forming transfer hydrogenation

1 reference

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Elongation of 1,3-polyols via iterative catalyst-directed carbonyl allylation from the alcohol oxidation level

1 reference

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1,n-glycols as dialdehyde equivalents in iridium-catalyzed enantioselective carbonyl allylation and iterative two-directional assembly of 1,3-polyols

1 reference

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Enantioselective carbonyl reverse prenylation from the alcohol or aldehyde oxidation level employing 1,1-dimethylallene as the prenyl donor

1 reference

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Impact of natural products on developing new anti-cancer agents

1 reference

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5 July 2018

Redox economy in organic synthesis

1 reference

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Biosynthesis of aromatic polyketides in bacteria

1 reference

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Combinatorial biosynthesis of plant medicinal polyketides by microorganisms

1 reference

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5 July 2018

anti-Diastereo- and enantioselective carbonyl crotylation from the alcohol or aldehyde oxidation level employing a cyclometallated iridium catalyst: alpha-methyl allyl acetate as a surrogate to preformed crotylmetal reagents

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975273

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The biosynthesis of polyketide-derived polycyclic ethers

1 reference

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Catalytic carbonyl addition through transfer hydrogenation: a departure from preformed organometallic reagents

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975273

5 July 2018

Engineering of plant polyketide biosynthesis

1 reference

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5 July 2018

Enantioselective iridium-catalyzed carbonyl allylation from the alcohol or aldehyde oxidation level via transfer hydrogenative coupling of allyl acetate: departure from chirally modified allyl metal reagents in carbonyl addition

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975273

5 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=2975273

5 July 2018

Advances in polyketide synthase structure and function.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975273

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Natural products as sources of new drugs over the last 25 years

1 reference

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Type II polyketide synthases: gaining a deeper insight into enzymatic teamwork

1 reference

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Stereoselective synthesis of the C(1)-C(19) fragment of tetrafibricin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975273

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Modern aldol methods for the total synthesis of polyketides

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975273

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Large-scale oxidations in the pharmaceutical industry

1 reference

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Advances in the total synthesis of biologically important marine macrolides

1 reference

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1 reference

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Genetic approaches to polyketide antibiotics. 1.

1 reference

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Metabolic engineering for drug discovery and development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975273

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Biosynthesis of polyketides and related compounds

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975273

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Concise synthesis of the bryostatin A-ring via consecutive C-C bond forming transfer hydrogenations

1 reference

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Amplification of asymmetric induction in sequential reactions of bis-diazoacetates catalyzed by chiral dirhodium(II) carboxamidates.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975273

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Total synthesis of the polyene-polyol macrolide RK-397, featuring cross-couplings of alkynylepoxide modules.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975273

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975273

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975273

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975273

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Total synthesis of (+)-phorboxazole A exploiting the Petasis-Ferrier rearrangement

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975273

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Formal total synthesis of mycoticin A.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2975273

28 October 2018

A New Role for Polyketides

1 reference

https://pubmed.ncbi.nlm.nih.gov/20961111

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Total synthesis of RK-397

1 reference

https://pubmed.ncbi.nlm.nih.gov/20961111

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The total synthesis of the oxopolyene macrolide RK-397

1 reference

https://pubmed.ncbi.nlm.nih.gov/20961111

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Marine natural products: synthetic aspects

1 reference

https://pubmed.ncbi.nlm.nih.gov/20961111

12 December 2020

based on heuristic

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20961111

12 December 2020

based on heuristic

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Formal synthesis of (+)-SCH 351448: the Prins cyclization approach

1 reference

https://pubmed.ncbi.nlm.nih.gov/20961111

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/20961111

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Formal total synthesis of RK-397 via an asymmetric hydration and iterative allylation strategy

1 reference

https://pubmed.ncbi.nlm.nih.gov/20961111

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Total Synthesis of Dermostatin A

1 reference

https://pubmed.ncbi.nlm.nih.gov/20961111

12 December 2020

based on heuristic

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Identifiers

10.1021/JA1082798

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Europe PubMed Central

31 July 2017

release_dpprkyukhzdr7bgkn4gj2s5cme

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https://api.fatcat.wiki/v0/release/dpprkyukhzdr7bgkn4gj2s5cme

24 November 2022

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31 July 2017

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Europe PubMed Central

31 July 2017

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