Stereoselectivity in intramolecular 1,3-dipolar cycloadditions. Nitrile oxides versus silyl nitronates

W. Dehaen, A. Hassner

Research output: Contribution to journalArticlepeer-review

53 Scopus citations

Abstract

Unlike nitrile oxides, silyl nitronates undergo highly stereoselective intramolecular cycloadditions to produce functionalized carbocyclic or heterocyclic rings.

Original languageEnglish
Pages (from-to)743-746
Number of pages4
JournalTetrahedron Letters
Volume31
Issue number5
DOIs
StatePublished - 1990

Bibliographical note

Funding Information:
Acknowledgement:S upport of this research by Grant 87-00299 from the US-Israel Binational Science Foundation is gratefully acknowleged. We thank Dr. H.E. Gottlieb for valuable help with NMRs pectra.

Funding

Acknowledgement:S upport of this research by Grant 87-00299 from the US-Israel Binational Science Foundation is gratefully acknowleged. We thank Dr. H.E. Gottlieb for valuable help with NMRs pectra.

FundersFunder number
United States-Israel Binational Science Foundation

    Fingerprint

    Dive into the research topics of 'Stereoselectivity in intramolecular 1,3-dipolar cycloadditions. Nitrile oxides versus silyl nitronates'. Together they form a unique fingerprint.

    Cite this