A novel organic electron donor derived from N-methylisatin

Ryan  Sword; Steven O'Sullivan; John A Murphy

doi:10.1071/CH12480

A novel organic electron donor derived from N-methylisatin

Ryan Sword, Steven O'Sullivan, John A Murphy

Pure And Applied Chemistry

Research output: Contribution to journal › Article › peer-review

11 Citations (Scopus)

Abstract

We report the reactivity of an electron donor derived from N-methylisatin on reduction by sodium amalgam. Transfer of a clear supernatant solution to iodoarenes affords the products of two-electron reduction. Reductions of sulfones, activated arenesulfonamides, and Weinreb amides are also reported.

Original language	English
Pages (from-to)	314-322
Number of pages	9
Journal	Australian Journal of Chemistry
Volume	66
Issue number	3
DOIs	https://doi.org/10.1071/CH12480
Publication status	Published - 7 Jan 2013

Keywords

sulfones
electron donor
N-methylisatin

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10.1071/CH12480

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1 Finished

Pathways to Impact Award
Littlejohn, D., Cross, A., Phelps, A. & Ronald, K.
EPSRC (Engineering and Physical Sciences Research Council)
1/08/10 → 31/03/11
Project: Research

Cite this

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abstract = "We report the reactivity of an electron donor derived from N-methylisatin on reduction by sodium amalgam. Transfer of a clear supernatant solution to iodoarenes affords the products of two-electron reduction. Reductions of sulfones, activated arenesulfonamides, and Weinreb amides are also reported.",

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AB - We report the reactivity of an electron donor derived from N-methylisatin on reduction by sodium amalgam. Transfer of a clear supernatant solution to iodoarenes affords the products of two-electron reduction. Reductions of sulfones, activated arenesulfonamides, and Weinreb amides are also reported.

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JF - Australian Journal of Chemistry

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A novel organic electron donor derived from N-methylisatin

Abstract

Keywords

Access to Document

Pathways to Impact Award

Cite this