Theoretical studies of a singlet oxygen-releasing dioxapaddlane (1,4-diicosa naphthalene-1,4-endoperoxide)

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Probing the reactivity of singlet oxygen with purines.New singlet oxygen donors based on naphthalenes: synthesis, physical chemical data, and improved stability.

P2860

Q27324862-30A6DCD3-634D-4EBC-9C86-2F0274F2F6C5 Q30940206-AB0DEE80-0222-47AB-BFE1-7339515F9BA8

P2860

Theoretical studies of a singlet oxygen-releasing dioxapaddlane (1,4-diicosa naphthalene-1,4-endoperoxide)

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http://www.wikidata.org/entity/Q41832942

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2009 nî lūn-bûn

@nan

2009年の論文

@ja

2009年論文

@yue

2009年論文

@zh-hant

2009年論文

@zh-hk

2009年論文

@zh-mo

2009年論文

@zh-tw

2009年论文

@wuu

2009年论文

@zh

2009年论文

@zh-cn

name

Theoretical studies of a singl ...... naphthalene-1,4-endoperoxide)

@en

type

Item

label

Theoretical studies of a singl ...... naphthalene-1,4-endoperoxide)

@en

prefLabel

Theoretical studies of a singl ...... naphthalene-1,4-endoperoxide)

@en

P1476

Theoretical studies of a singl ...... naphthalene-1,4-endoperoxide)

@en

P2093

Alvaro Castillo

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

P2860

Quantitative determination of singlet oxygen generated by excited state aromatic amino acids, proteins, and immunoglobulins.

Spin conservation accounts for aluminum cluster anion reactivity pattern with O2.

Overview of theoretical and computational methods applied to the oxygen-organic molecule photosystem.

Reactivity within a confined self-assembled nanospace.

Reactions of 1,3-cyclohexadiene with singlet oxygen. A theoretical study.

Formation of a nonaoxirane from A2E, a lipofuscin fluorophore related to macular degeneration, and evidence of singlet oxygen involvement.

Mechanism of ene reactions of singlet oxygen. A two-step no-intermediate mechanism.

H-bond-assisted regioselective (cis-1) intramolecular nucleophilic addition of the hydroxyl group to [60]fullerene.

Theoretical prediction of a perepoxide intermediate for the reaction of singlet oxygen with trans-cyclooctene contrasts with the two-step no-intermediate ene reaction for acyclic alkenes.

Inherently chiral uranyl-salophen macrocycles: computer-aided design and resolution.

P2888

s11224-009-9424-1

P304

399-407

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P31

scholarly article

P356

10.1007/S11224-009-9424-1

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P433

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

P478

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

P50

Alexander Greer

P577

2009-06-01T00:00:00Z

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P5875

230645783

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P6179

1011847942

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P698

22879733

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P932

3413292

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Theoretical studies of a singlet oxygen-releasing dioxapaddlane (1,4-diicosa naphthalene-1,4-endoperoxide)

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P2860

P2860

Theoretical studies of a singlet oxygen-releasing dioxapaddlane (1,4-diicosa naphthalene-1,4-endoperoxide)

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P5875

P6179

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P5875

P6179

P698

P932