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    Rights statement: This is the author’s version of a work that was accepted for publication in Tetrahedron. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Tetrahedron, 73 1, 2016 DOI: 10.1016/j.tet.2016.11.060

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Synthesis and substrate-controlled reactions of 2,2′-Unsaturated biquinazolinones

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<mark>Journal publication date</mark>5/01/2017
<mark>Journal</mark>Tetrahedron
Issue number1
Volume73
Number of pages9
Pages (from-to)55-63
StatePublished
Early online date23/11/16
Original languageEnglish

Abstract

A series of BiQuinazolinones bearing either double or triple bonds in their lateral chains have been synthesized. These compounds were then subjected to substrate-controlled reactions such as Diels-Alder, epoxidation and Pauson-Khand reactions. The stereoselective outcome observed in these transformations is very promising for the future application of BiQuinazolinones as chiral auxiliaries.

Bibliographic note

This is the author’s version of a work that was accepted for publication in Tetrahedron. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Tetrahedron, 73, 1, 2016 DOI: 10.1016/j.tet.2016.11.060