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Literature DB >> 17939662

Reductive cleavage of sulfones and sulfonamides by a neutral organic super-electron-donor (S.E.D.) reagent.

Franziska Schoenebeck¹, John A Murphy, Sheng-ze Zhou, Yoshitaka Uenoyama, Yves Miclo, Tell Tuttle.

Abstract

Entities: Chemical Species

Mesh：

Substances：

Year: 2007 PMID： 17939662 DOI： 10.1021/ja074417h

Source DB: PubMed Journal: J Am Chem Soc ISSN： 0002-7863 Impact factor: 15.419

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18 in total

1. Studies toward the oxidative and reductive activation of C-S bonds in 2'-S-aryl-2'-thiouridine derivatives.

Authors: Ramanjaneyulu Rayala; Alain Giuglio-Tonolo; Julie Broggi; Thierry Terme; Patrice Vanelle; Patricia Theard; Maurice Médebielle; Stanislaw F Wnuk
Journal: Tetrahedron Date: 2016-04-21 Impact factor: 2.457

2. Iron-catalyzed cross-coupling of unactivated secondary alkyl thio ethers and sulfones with aryl Grignard reagents.

Authors: Scott E Denmark; Alexander J Cresswell
Journal: J Org Chem Date: 2013-11-20 Impact factor: 4.354

3. Red Light-Based Dual Photoredox Strategy Resembling the Z-Scheme of Natural Photosynthesis.

Authors: Felix Glaser; Oliver S Wenger
Journal: JACS Au Date: 2022-06-10

4. Hybrid super electron donors - preparation and reactivity.

Authors: Jean Garnier; Douglas W Thomson; Shengze Zhou; Phillip I Jolly; Leonard E A Berlouis; John A Murphy
Journal: Beilstein J Org Chem Date: 2012-07-03 Impact factor: 2.883

5. Reductions of challenging organic substrates by a nickel complex of a noninnocent crown carbene ligand.

Authors: Neil J Findlay; Stuart R Park; Franziska Schoenebeck; Elise Cahard; Sheng-Ze Zhou; Leonard E A Berlouis; Mark D Spicer; Tell Tuttle; John A Murphy
Journal: J Am Chem Soc Date: 2010-11-10 Impact factor: 15.419

6. Overturning established chemoselectivities: selective reduction of arenes over malonates and cyanoacetates by photoactivated organic electron donors.

Authors: Eswararao Doni; Bhaskar Mondal; Steven O'Sullivan; Tell Tuttle; John A Murphy
Journal: J Am Chem Soc Date: 2013-07-19 Impact factor: 15.419

Reductive cleavage of sulfones and sulfonamides by a neutral organic super-electron-donor (S.E.D.) reagent.

1. Studies toward the oxidative and reductive activation of C-S bonds in 2'-S-aryl-2'-thiouridine derivatives.

2. Iron-catalyzed cross-coupling of unactivated secondary alkyl thio ethers and sulfones with aryl Grignard reagents.

3. Red Light-Based Dual Photoredox Strategy Resembling the Z-Scheme of Natural Photosynthesis.

4. Hybrid super electron donors - preparation and reactivity.

5. Reductions of challenging organic substrates by a nickel complex of a noninnocent crown carbene ligand.

6. Overturning established chemoselectivities: selective reduction of arenes over malonates and cyanoacetates by photoactivated organic electron donors.

7. Structure and reactivity in neutral organic electron donors derived from 4-dimethylaminopyridine.

8. Amidine dications as superelectrophiles.

9. One-carbon extrusion from a tetraazafulvalene. Isolation of aldehydes and a study of their origin.

10. Pushing the limits of neutral organic electron donors: a tetra(iminophosphorano)-substituted bispyridinylidene.