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

10 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

Access to Document

10.1071/CH12480

Link to publication in Scopus

Fingerprint Dive into the research topics of 'A novel organic electron donor derived from N-methylisatin'. Together they form a unique fingerprint.

Projects

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

Sword, R., O'Sullivan, S., & Murphy, J. A. (2013). A novel organic electron donor derived from N-methylisatin. Australian Journal of Chemistry, 66(3), 314-322. https://doi.org/10.1071/CH12480

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