(Q37660116)

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

scientific article published on 16 October 2009

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scholarly article

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Europe PubMed Central

PMC publication ID

21 August 2017

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Europe PubMed Central

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

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Europe PubMed Central

PMC publication ID

21 August 2017

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enantioselectivity

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based on heuristic

inferred from title

Michael J. Krische

3

object named as

Michael J Krische

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Europe PubMed Central

21 August 2017

PMC publication ID

author name string

Soo Bong Han

1

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Europe PubMed Central

PMC publication ID

21 August 2017

In Su Kim

2

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Europe PubMed Central

PMC publication ID

21 August 2017

language of work or name

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publication date

16 October 2009

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Europe PubMed Central

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21 August 2017

Chemical Communications

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Europe PubMed Central

PMC publication ID

21 August 2017

47

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Europe PubMed Central

PMC publication ID

21 August 2017

7278-7287

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Redox economy in organic synthesis

1 reference

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Heterogeneous photocatalyst materials for water splitting

1 reference

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

1 reference

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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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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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Iridium-catalyzed C-C coupling via transfer hydrogenation: carbonyl addition from the alcohol or aldehyde oxidation level employing 1,3-cyclohexadiene

1 reference

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Catalytic asymmetric generation of (Z)-disubstituted allylic alcohols

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Total Synthesis of Bryostatin 3

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The atom economy--a search for synthetic efficiency

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

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

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Catalytic C-C coupling via transfer hydrogenation: reverse prenylation, crotylation, and allylation from the alcohol or aldehyde oxidation level

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

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

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1 reference

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1 reference

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Total synthesis of the L-hexoses

1 reference

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Chemistry. Rethinking water splitting

1 reference

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1 reference

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Identifiers

10.1039/B917243M

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

ResearchGate publication ID

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