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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

Research output: Contribution to Journal/Magazine › Journal article › peer-review

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Synthesis and substrate-controlled reactions of 2,2′-Unsaturated biquinazolinones. / Pertusati, Fabrizio; Nutz, Eva; Kariuki, Benson M. et al.
In: Tetrahedron, Vol. 73, No. 1, 05.01.2017, p. 55-63.

Research output: Contribution to Journal/Magazine › Journal article › peer-review

Harvard

Pertusati, F, Nutz, E, Kariuki, BM & Coogan, MP 2017, 'Synthesis and substrate-controlled reactions of 2,2′-Unsaturated biquinazolinones', Tetrahedron, vol. 73, no. 1, pp. 55-63. https://doi.org/10.1016/j.tet.2016.11.060

APA

Pertusati, F., Nutz, E., Kariuki, B. M., & Coogan, M. P. (2017). Synthesis and substrate-controlled reactions of 2,2′-Unsaturated biquinazolinones. Tetrahedron, 73(1), 55-63. https://doi.org/10.1016/j.tet.2016.11.060

Vancouver

Pertusati F, Nutz E, Kariuki BM, Coogan MP. Synthesis and substrate-controlled reactions of 2,2′-Unsaturated biquinazolinones. Tetrahedron. 2017 Jan 5;73(1):55-63. Epub 2016 Nov 23. doi: 10.1016/j.tet.2016.11.060

Author

Pertusati, Fabrizio ; Nutz, Eva ; Kariuki, Benson M. et al. / Synthesis and substrate-controlled reactions of 2,2′-Unsaturated biquinazolinones. In: Tetrahedron. 2017 ; Vol. 73, No. 1. pp. 55-63.

Bibtex

@article{cdd1f7e986d64ed5a13d9fb972363a39,
title = "Synthesis and substrate-controlled reactions of 2,2′-Unsaturated biquinazolinones",
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.",
keywords = "BiQuinazolinone, Atropisomers, Diastereoselectivity, Chiral induction",
author = "Fabrizio Pertusati and Eva Nutz and Kariuki, {Benson M.} and Coogan, {Michael Peter}",
note = "This is the author{\textquoteright}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",
year = "2017",
month = jan,
day = "5",
doi = "10.1016/j.tet.2016.11.060",
language = "English",
volume = "73",
pages = "55--63",
journal = "Tetrahedron",
issn = "0040-4020",
publisher = "Elsevier Limited",
number = "1",

}

RIS

TY - JOUR

T1 - Synthesis and substrate-controlled reactions of 2,2′-Unsaturated biquinazolinones

AU - Pertusati, Fabrizio

AU - Nutz, Eva

AU - Kariuki, Benson M.

AU - Coogan, Michael Peter

N1 - 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

PY - 2017/1/5

Y1 - 2017/1/5

N2 - 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.

AB - 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.

KW - BiQuinazolinone

KW - Atropisomers

KW - Diastereoselectivity

KW - Chiral induction

U2 - 10.1016/j.tet.2016.11.060

DO - 10.1016/j.tet.2016.11.060

M3 - Journal article

VL - 73

SP - 55

EP - 63

JO - Tetrahedron

JF - Tetrahedron

SN - 0040-4020

IS - 1

ER -