Aza-oxindole synthesis via base promoted Truce–Smiles rearrangement

Dey, Chandan; Katayev, Dmitry; Ylijoki, Kai Erik Oskar; Kundig, Ernst Peter

doi:10.1039/c2cc36068c

Scientific article

English

Aza-oxindole synthesis via base promoted Truce–Smiles rearrangement

ContributorsDey, Chandan; Katayev, Dmitry; Ylijoki, Kai Erik Oskar; Kundig, Ernst Peter

Published inChemical communications, vol. 48, no. 89, p. 10957-10959

Publication date2012

Abstract

A novel efficient NaOtBu-mediated protocol for the synthesis of 3,3-disubstituted aza-oxindoles proceeds via a Truce–Smiles rearrangement–cyclisation pathway.

Affiliation entities

Faculté des sciences / Section de chimie et biochimie / Département de chimie organique

Citation (ISO format)

DEY, Chandan et al. Aza-oxindole synthesis via base promoted Truce–Smiles rearrangement. In: Chemical communications, 2012, vol. 48, n° 89, p. 10957–10959. doi: 10.1039/c2cc36068c

Article (Published version)

Identifiers

PID : unige:23521
DOI : 10.1039/c2cc36068c

Additional URL for this publicationhttp://xlink.rsc.org/?DOI=c2cc36068c

Journal ISSN1359-7345

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Aza-oxindole synthesis via base promoted Truce–Smiles rearrangement

A novel efficient NaOtBu-mediated protocol for the synthesis of 3,3-disubstituted aza-oxindoles proceeds via a Truce–Smiles rearrangement–cyclisation pathway.

Technical informations