Concepedia

A mild and efficient method for the synthesis of a new optically active diallyl selenide and its catalytic activity in the allylic chlorination of natural terpenes

Brahim Boualy, Soufiane El Houssame, Luca Sancineto, Claudio Santi, Mustapha Ait Ali, H. Stoeckli‐Evans, Larbi El Firdoussi

New Journal of Chemistry · 2016 · 19 citations · 19 references

DOI

Concepts

Abstract

An organoselenide compound was synthesized starting from β-pinene. The activity of this complex towards allylic chlorination has been studied.

References

19

A short history of<i>SHELX</i>

George M. Sheldrick · Acta Crystallographica Section A Foundations of Crystallography · 2007 · 87.4K citations · Full text

, , +16

Structure validation in chemical crystallography

Anthony L. Spek · Acta Crystallographica Section D Biological Crystallography · 2009 · 15.3K citations · Full text

, , +16

Recent developments in the chemistry of selenoethers and telluroethers

William Levason, S.D. Orchard, Gillian Reid · Coordination Chemistry Reviews · 2002 · 214 citations

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Metal Chalcogenide Materials: Chalcogenolato complexes as “single‐source” precursors

Manfred Bochmann · Chemical Vapor Deposition · 1996 · 185 citations

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MOCVD of Chalcogenides, Pnictides, and Heterometallic Compounds from Single-Source Molecule Precursors

Alain Gleizes · Chemical Vapor Deposition · 2000 · 127 citations

, , +12