(Q34103647)

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

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Europe PubMed Central

PubMed publication ID

31 July 2017

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

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Europe PubMed Central

PubMed publication ID

31 July 2017

enantioselectivity

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Michael J. Krische

4

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Michael J Krische

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31 July 2017

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Yong Jian Zhang

1

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31 July 2017

Jin Haek Yang

2

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31 July 2017

Sang Hoon Kim

3

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31 July 2017

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publication date

1 April 2010

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31 July 2017

Journal of the American Chemical Society

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31 July 2017

132

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31 July 2017

13

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31 July 2017

4562-4563

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Europe PubMed Central

PubMed publication ID

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

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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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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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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

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

1 reference

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Total syntheses of (+)-tedanolide and (+)-13-deoxytedanolide

1 reference

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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

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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

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

1 reference

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

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Total synthesis of natural myriaporones

1 reference

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Catalytic Enantioselective Addition of Allylic Organometallic Reagents to Aldehydes and Ketones

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The total synthesis of (+)-tedanolide--A macrocyclic polyketide from marine sponge Tedania ignis

1 reference

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12 December 2020

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Umpolung of vinyloxiranes: regio- and stereoselectivity of the In/Pd-mediated allylation of carbonyl compounds

1 reference

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12 December 2020

based on heuristic

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Creation of quaternary stereocenters in carbonyl allylation reactions

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Total Synthesis of (+)-Tedanolide

1 reference

https://pubmed.ncbi.nlm.nih.gov/20225853

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

One-pot enantioselective synthesis of optically active homoallylic alcohols from allyl halides

1 reference

https://pubmed.ncbi.nlm.nih.gov/20225853

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Total synthesis of (+)-13-deoxytedanolide

1 reference

https://pubmed.ncbi.nlm.nih.gov/20225853

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Total synthesis of (+)-tedanolide

1 reference

https://pubmed.ncbi.nlm.nih.gov/20225853

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1021/JA100949E

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

ResearchGate publication ID

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