Sodium Diisopropylamide in Tetrahydrofuran: Selectivities, Rates, and Mechanisms of Alkene Isomerizations and Diene Metalations.

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Sodium Diisopropylamide in Tetrahydrofuran: Selectivities, Rates, and Mechanisms of Arene Metalations.

P2860

Q48293156-1C641D93-7C4A-4D55-813B-0A4CE81D2252

P2860

Sodium Diisopropylamide in Tetrahydrofuran: Selectivities, Rates, and Mechanisms of Alkene Isomerizations and Diene Metalations.

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http://www.wikidata.org/entity/Q38666197

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

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2017年學術文章

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2017年學術文章

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name

Sodium Diisopropylamide in Tet ...... zations and Diene Metalations.

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type

Item

label

Sodium Diisopropylamide in Tet ...... zations and Diene Metalations.

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prefLabel

Sodium Diisopropylamide in Tet ...... zations and Diene Metalations.

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P1476

Sodium Diisopropylamide in Tet ...... zations and Diene Metalations.

@en

P2093

Russell F Algera

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Yun Ma

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P2860

Concise asymmetric total synthesis of scyphostatin, a potent inhibitor of neutral sphingomyelinase

Lithium hexamethyldisilazide-mediated enolizations: influence of triethylamine on E/Z selectivities and enolate reactivities.

Lithium diisopropylamide: solution kinetics and implications for organic synthesis.

In situ FTIR reaction analysis of pharmaceutical-related chemistry and processes.

Sodium Diisopropylamide in N,N-Dimethylethylamine: Reactivity, Selectivity, and Synthetic Utility

A method for the preparation of differentiated trans-1,2-diol derivatives with enantio- and diastereocontrol.

Isomerization of allyl ethers initiated by lithium diisopropylamide.

Synthetically important alkali-metal utility amides: lithium, sodium, and potassium hexamethyldisilazides, diisopropylamides, and tetramethylpiperidides.

Concerted rearrangement versus heterolytic cleavage in anionic [2,3]- and [3,3]-sigmatropic shifts. A DFT study of relationships among anion stabilities, mechanisms, and rates.

Lithium hexamethyldisilazide/triethylamine-mediated ketone enolization: remarkable rate accelerations stemming from a dimer-based mechanism.

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11544-11549

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scholarly article

P356

10.1021/JACS.7B05218

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English

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139

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David B Collum

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2017-07-22T00:00:00Z

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28735535

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6059566

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Sodium Diisopropylamide in Tetrahydrofuran: Selectivities, Rates, and Mechanisms of Alkene Isomerizations and Diene Metalations.

about

P2860

P2860

Sodium Diisopropylamide in Tetrahydrofuran: Selectivities, Rates, and Mechanisms of Alkene Isomerizations and Diene Metalations.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932