Direct Copper-Free Domino Conjugate Addition-Cycloallylation using Organozinc Reagents

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Advances in tandem reactions with organozinc reagents.Stereogenic-at-metal Zn- and Al-based N-heterocyclic carbene (NHC) complexes as bifunctional catalysts in Cu-free enantioselective allylic alkylations.

P2860

Q38364611-8F50760B-D7DE-41E1-90F3-AB30D9CF1835 Q41837498-5D522CF5-D9F9-46FB-AB9C-EDB52BF5A9E8

P2860

Direct Copper-Free Domino Conjugate Addition-Cycloallylation using Organozinc Reagents

Item

http://www.wikidata.org/entity/Q40384958

description

2008 nî lūn-bûn

@nan

2008年の論文

@ja

2008年論文

@yue

2008年論文

@zh-hant

2008年論文

@zh-hk

2008年論文

@zh-mo

2008年論文

@zh-tw

2008年论文

@wuu

2008年论文

@zh

2008年论文

@zh-cn

name

Direct Copper-Free Domino Conjugate Addition-Cycloallylation using Organozinc Reagents

@en

type

Item

label

Direct Copper-Free Domino Conjugate Addition-Cycloallylation using Organozinc Reagents

@en

prefLabel

Direct Copper-Free Domino Conjugate Addition-Cycloallylation using Organozinc Reagents

@en

P1476

Direct Copper-Free Domino Conjugate Addition-Cycloallylation using Organozinc Reagents

@en

P2093

Fernando Pedraza

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

Venukrishnan Komanduri

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

P2860

Palladium-Catalyzed Asymmetric Allylic α-Alkylation of Acyclic Ketones

Phosphoramidites: marvellous ligands in catalytic asymmetric conjugate addition.

Catalytic asymmetric tandem transformations triggered by conjugate additions.

Desymmetrization of enone-diones via rhodium-catalyzed diastereo- and enantioselective tandem conjugate addition-aldol cyclization.

Diastereoselective cycloreductions and cycloadditions catalyzed by Co(dpm)(2)-silane (dpm = 2,2,6,6-tetramethylheptane-3,5-dionate): mechanism and partitioning of hydrometallative versus anion radical pathways.

A new type of catalytic tandem 1,4-addition-aldol reaction which proceeds through an (oxa-pi-allyl)rhodium intermediate.

Catalytic enantioselective synthesis of (-)-prostaglandin E1 methyl ester based on a tandem 1,4-addition-aldol reaction.

Borane-mediated aldol cycloreduction of monoenone monoketones: diastereoselective formation of quaternary centers.

Catalytic enone cycloallylation via concomitant activation of latent nucleophilic and electrophilic partners: merging organic and transition metal catalysis.

Migratory hydroamination: a facile enantioselective synthesis of benzomorphans.

P304

1569-1576

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P31

scholarly article

P356

10.1002/ADSC.200800242

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

P433

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

P478

350

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P50

Michael J. Krische

P577

2008-07-01T00:00:00Z

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

P5875

44584564

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P698

20454546

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

P932

2865154

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

Direct Copper-Free Domino Conjugate Addition-Cycloallylation using Organozinc Reagents

about

P2860

P2860

Direct Copper-Free Domino Conjugate Addition-Cycloallylation using Organozinc Reagents

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P932