Alkyne-aldehyde reductive C-C coupling through ruthenium-catalyzed transfer hydrogenation: direct regio- and stereoselective carbonyl vinylation to form trisubstituted allylic alcohols in the absence of premetallated reagents.

Alkyne-aldehyde reductive C-C coupling through ruthenium-catalyzed transfer hydrogenation: direct regio- and stereoselective carbonyl vinylation to form trisubstituted allylic alcohols in the absence of premetallated reagents.

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http://www.wikidata.org/entity/Q39021555

Q39021555

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Nickel-catalyzed cycloaddition of 1,3-dienes with 3-azetidinones and 3-oxetanones.Formation of C-C bonds via ruthenium-catalyzed transfer hydrogenation().Enantioselective ruthenium-catalyzed carbonyl allylation via alkyne-alcohol C-C bond-forming transfer hydrogenation: allene hydrometalation vs oxidative coupling.Redox-triggered C-C coupling of diols and alkynes: synthesis of β,γ-unsaturated α-hydroxyketones and furans by ruthenium-catalyzed hydrohydroxyalkylation.Total Synthesis of Oridamycins A and B.Alkynes as allylmetal equivalents in redox-triggered C-C couplings to primary alcohols: (Z)-homoallylic alcohols via ruthenium-catalyzed propargyl C-H oxidative addition.Catalytic Hydroalkylation of Allenes.

P2860

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P2860

Alkyne-aldehyde reductive C-C coupling through ruthenium-catalyzed transfer hydrogenation: direct regio- and stereoselective carbonyl vinylation to form trisubstituted allylic alcohols in the absence of premetallated reagents.

Item

http://www.wikidata.org/entity/Q39021555

description

2011 nî lūn-bûn

@nan

2011年の論文

@ja

2011年論文

@yue

2011年論文

@zh-hant

2011年論文

@zh-hk

2011年論文

@zh-mo

2011年論文

@zh-tw

2011年论文

@wuu

2011年论文

@zh

2011年论文

@zh-cn

name

Alkyne-aldehyde reductive C-C ...... nce of premetallated reagents.

@en

Alkyne-aldehyde reductive C-C ...... nce of premetallated reagents.

@nl

type

Item

label

Alkyne-aldehyde reductive C-C ...... nce of premetallated reagents.

@en

Alkyne-aldehyde reductive C-C ...... nce of premetallated reagents.

@nl

prefLabel

Alkyne-aldehyde reductive C-C ...... nce of premetallated reagents.

@en

Alkyne-aldehyde reductive C-C ...... nce of premetallated reagents.

@nl

P1476

Alkyne-aldehyde reductive C-C ...... nce of premetallated reagents.

@en

P2093

Brannon Sam

http://www.w3.org/2001/XMLSchema#string

Joyce C Leung

http://www.w3.org/2001/XMLSchema#string

Ryan L Patman

http://www.w3.org/2001/XMLSchema#string

P2860

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

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

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

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

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

Enantioselective iridium-catalyzed carbonyl allylation from the alcohol or aldehyde oxidation level using allyl acetate as an allyl metal surrogate

Ruthenium-catalyzed C-C bond forming transfer hydrogenation: carbonyl allylation from the alcohol or aldehyde oxidation level employing acyclic 1,3-dienes as surrogates to preformed allyl metal reagents.

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

Mechanism and origins of regio- and enantioselectivities in RhI-catalyzed hydrogenative couplings of 1,3-diynes and activated carbonyl partners: intervention of a cumulene intermediate

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

P304

12437-12443

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P31

scholarly article

P356

10.1002/CHEM.201101554

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P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

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P50

Michael J. Krische

P577

2011-09-27T00:00:00Z

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P5875

51668251

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21953608

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P921

stereoselectivity

P932

3212945

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Alkyne-aldehyde reductive C-C coupling through ruthenium-catalyzed transfer hydrogenation: direct regio- and stereoselective carbonyl vinylation to form trisubstituted allylic alcohols in the absence of premetallated reagents.

about

P2860

P2860

Alkyne-aldehyde reductive C-C coupling through ruthenium-catalyzed transfer hydrogenation: direct regio- and stereoselective carbonyl vinylation to form trisubstituted allylic alcohols in the absence of premetallated reagents.

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P1433

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P2860

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P356

P407

P433

P478

P50

P577

P5875

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P921

P932

P356

P1433

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P356

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P433

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P921

P932