ChemInform Abstract: Singlet-Triplet Mechanistic Duality in the Photosubstitution of Nitrophenyl Ethers with Ethyl Glycinate. The Role of Single Electron Transfer.

10.1002/chin.199221102 ◽

2010 ◽

Vol 23 (21) ◽

pp. no-no

Author(s):

J. MARQUET ◽

A. CANTOS ◽

M. MORENO-MANAS ◽

E. CAYON ◽

I. GALLARDO

Keyword(s):

Electron Transfer ◽

Single Electron ◽

Single Electron Transfer

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ChemInform Abstract: Dual Role of Allylsamarium Bromide as a Grignard Reagent and a Single Electron Transfer Reagent in the One-Pot Synthesis of Terminal Olefins.

10.1002/chin.201410062 ◽

2014 ◽

Vol 45 (10) ◽

pp. no-no

Author(s):

Ying Li ◽

Yuan-Yuan Hu ◽

Song-Lin Zhang

Keyword(s):

Electron Transfer ◽

Grignard Reagent ◽

Dual Role ◽

Single Electron ◽

Single Electron Transfer ◽

One Pot ◽

One Pot Synthesis ◽

The One ◽

Terminal Olefins

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ChemInform Abstract: Unexpected Mild Protection of Alcohols as 2-O-THF and 2-O-THP Ethers Catalyzed by Cp2TiCl Reveal an Intriguing Role of the Solvent in the Single-Electron Transfer Reaction.

10.1002/chin.201607072 ◽

2016 ◽

Vol 47 (7) ◽

pp. no-no

Author(s):

Maria Jesus Duran-Pena ◽

Jose Manuel Botubol-Ares ◽

James R. Hanson ◽

Rosario Hernandez-Galan ◽

Isidro G. Collado

Keyword(s):

Electron Transfer ◽

Transfer Reaction ◽

Electron Transfer Reaction ◽

Single Electron ◽

Single Electron Transfer ◽

Single Electron Transfer Reaction

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Singlet-triplet mechanistic duality in the photosubstitution of nitrophenyl ethers with ethyl glycinate. The role of single electron transfer.

Tetrahedron ◽

10.1016/s0040-4020(01)90795-1 ◽

1992 ◽

Vol 48 (7) ◽

pp. 1333-1342 ◽

Author(s):

Jorge Marquet ◽

Albert Cantos ◽

Marcial Moreno-Mañas ◽

Eduard Caýon ◽

Iluminada Gallardo

Keyword(s):

Electron Transfer ◽

Single Electron ◽

Single Electron Transfer

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Dual role of allylsamarium bromide as a Grignard reagent and a single electron transfer reagent in the one-pot synthesis of terminal olefins

Chemical Communications ◽

10.1039/c3cc45611k ◽

2013 ◽

Vol 49 (90) ◽

pp. 10635 ◽

Author(s):

Ying Li ◽

Yuan-Yuan Hu ◽

Song-Lin Zhang

Keyword(s):

Electron Transfer ◽

Grignard Reagent ◽

Dual Role ◽

Single Electron ◽

Single Electron Transfer ◽

One Pot ◽

One Pot Synthesis ◽

The One ◽

Terminal Olefins

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Reactivity of 5,6-Dihydro-5-hydroxythymid-6-yl Generated via Photoinduced Single Electron Transfer and the Role of Cyclohexa-1,4-diene in the Photodeoxygenation Process

Journal of the American Chemical Society ◽

10.1021/ja00122a021 ◽

1995 ◽

Vol 117 (17) ◽

pp. 4894-4904 ◽

Author(s):

Mark R. Barvian ◽

Robert M. Barkley ◽

Marc M. Greenberg

Keyword(s):

Electron Transfer ◽

Single Electron ◽

Single Electron Transfer

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Role of single electron transfer in SN2-type substitution reactions of anions with alkyl halides

The Journal of Organic Chemistry ◽

10.1021/jo00281a035 ◽

1989 ◽

Vol 54 (20) ◽

pp. 4893-4898 ◽

Author(s):

F. G. Bordwell ◽

John A. Harrelson

Keyword(s):

Electron Transfer ◽

Alkyl Halides ◽

Single Electron ◽

Single Electron Transfer ◽

Substitution Reactions ◽

Type Substitution

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Unexpected Mild Protection of Alcohols as 2-O-THF and 2-O-THP Ethers Catalysed by Cp2TiCl Reveal an Intriguing Role of the Solvent in the Single-Electron Transfer Reaction

European Journal of Organic Chemistry ◽

10.1002/ejoc.201500869 ◽

2015 ◽

Vol 2015 (28) ◽

pp. 6333-6340 ◽

Author(s):

María Jesús Durán-Peña ◽

José Manuel Botubol-Ares ◽

James R. Hanson ◽

Rosario Hernández-Galán ◽

Isidro G. Collado

Keyword(s):

Electron Transfer ◽

Transfer Reaction ◽

Electron Transfer Reaction ◽

Single Electron ◽

Single Electron Transfer ◽

Single Electron Transfer Reaction

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ChemInform Abstract: ROLE OF SINGLE-ELECTRON TRANSFER IN SUBSTITUTION REACTIONS

Chemischer Informationsdienst ◽

10.1002/chin.197822338 ◽

1978 ◽

Vol 9 (22) ◽

Author(s):

Z. V. TODRES

Keyword(s):

Electron Transfer ◽

Single Electron ◽

Single Electron Transfer ◽

Substitution Reactions

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Evidence of single electron transfer from the enolate anion of an N,N′-dialkyldiketopiperazine additive in BHAS coupling reactions

Organic & Biomolecular Chemistry ◽

10.1039/c7ob02209c ◽

2017 ◽

Vol 15 (41) ◽

pp. 8810-8819 ◽

Author(s):

Katie J. Emery ◽

Tell Tuttle ◽

John A. Murphy

Keyword(s):

Electron Transfer ◽

Single Electron ◽

Single Electron Transfer ◽

Coupling Reactions ◽

Aromatic Substitution ◽

Substitution Reactions ◽

Homolytic Aromatic Substitution ◽

A designed N,N′-dialkyldiketopiperazine (DKP) provides evidence for the role of DKP additives as initiators that act by electron transfer in base-induced homolytic aromatic substitution reactions, involving coupling of haloarenes to arenes.

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The special role of B(C6F5)3 in the single electron reduction of quinones by radicals

Chemical Science ◽

10.1039/c8sc03005g ◽

2018 ◽

Vol 9 (41) ◽

pp. 8011-8018 ◽

Author(s):

Xin Tao ◽

Constantin G. Daniliuc ◽

Robert Knitsch ◽

Michael Ryan Hansen ◽

Hellmut Eckert ◽

...

Keyword(s):

Electron Transfer ◽

Radical Anion ◽

Single Electron ◽

Special Role ◽

Single Electron Transfer ◽

Electron Reduction ◽

In the presence of two molar equiv. of B(C6F5)3p-benzoquinone reacts with persistent radicals TEMPO, trityl or decamethylferrocene by single electron transfer to give the doubly O-borylated benzosemiquinone radical anion with TEMPO+, trityl cation or ferrocenium counter cations.

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