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Selective synthesis of three product classes from imine and carboxylic acid precursors via direct imine acylation

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Selective synthesis of three product classes from imine and carboxylic acid precursors via direct imine acylation. / Rossi-Ashton, James A; Taylor, Richard J K; Unsworth, William P.

In: Organic and Biomolecular Chemistry, Vol. 15, 05.09.2017, p. 7527-7532.

Research output: Contribution to journalArticle

Harvard

Rossi-Ashton, JA, Taylor, RJK & Unsworth, WP 2017, 'Selective synthesis of three product classes from imine and carboxylic acid precursors via direct imine acylation', Organic and Biomolecular Chemistry, vol. 15, pp. 7527-7532. https://doi.org/10.1039/c7ob02039b

APA

Rossi-Ashton, J. A., Taylor, R. J. K., & Unsworth, W. P. (2017). Selective synthesis of three product classes from imine and carboxylic acid precursors via direct imine acylation. Organic and Biomolecular Chemistry, 15, 7527-7532. https://doi.org/10.1039/c7ob02039b

Vancouver

Rossi-Ashton JA, Taylor RJK, Unsworth WP. Selective synthesis of three product classes from imine and carboxylic acid precursors via direct imine acylation. Organic and Biomolecular Chemistry. 2017 Sep 5;15:7527-7532. https://doi.org/10.1039/c7ob02039b

Author

Rossi-Ashton, James A ; Taylor, Richard J K ; Unsworth, William P. / Selective synthesis of three product classes from imine and carboxylic acid precursors via direct imine acylation. In: Organic and Biomolecular Chemistry. 2017 ; Vol. 15. pp. 7527-7532.

Bibtex - Download

@article{87ffd78eeecf43d08759c84c4d6700fd,
title = "Selective synthesis of three product classes from imine and carboxylic acid precursors via direct imine acylation",
abstract = "Three divergent Direct Imine Acylation (DIA) procedures are reported that allow the selective generation of δ-lactams, β-lactams and tetrahydropyrimidinones (via a novel three-component coupling) from imine and carboxylic acid precursors. All operate via initial N-acyliminium ion formation and diverge depending on the reaction conditions and nature of the substrates.",
keywords = "Journal Article",
author = "Rossi-Ashton, {James A} and Taylor, {Richard J K} and Unsworth, {William P}",
note = "{\circledC} The Royal Society of Chemistry 2017. This is an author-produced version of the published paper. Uploaded in accordance with the publisher’s self-archiving policy. Further copying may not be permitted; contact the publisher for details",
year = "2017",
month = "9",
day = "5",
doi = "10.1039/c7ob02039b",
language = "English",
volume = "15",
pages = "7527--7532",
journal = "Organic and Biomolecular Chemistry",
issn = "1477-0520",
publisher = "The Royal Society of Chemistry",

}

RIS (suitable for import to EndNote) - Download

TY - JOUR

T1 - Selective synthesis of three product classes from imine and carboxylic acid precursors via direct imine acylation

AU - Rossi-Ashton, James A

AU - Taylor, Richard J K

AU - Unsworth, William P

N1 - © The Royal Society of Chemistry 2017. This is an author-produced version of the published paper. Uploaded in accordance with the publisher’s self-archiving policy. Further copying may not be permitted; contact the publisher for details

PY - 2017/9/5

Y1 - 2017/9/5

N2 - Three divergent Direct Imine Acylation (DIA) procedures are reported that allow the selective generation of δ-lactams, β-lactams and tetrahydropyrimidinones (via a novel three-component coupling) from imine and carboxylic acid precursors. All operate via initial N-acyliminium ion formation and diverge depending on the reaction conditions and nature of the substrates.

AB - Three divergent Direct Imine Acylation (DIA) procedures are reported that allow the selective generation of δ-lactams, β-lactams and tetrahydropyrimidinones (via a novel three-component coupling) from imine and carboxylic acid precursors. All operate via initial N-acyliminium ion formation and diverge depending on the reaction conditions and nature of the substrates.

KW - Journal Article

U2 - 10.1039/c7ob02039b

DO - 10.1039/c7ob02039b

M3 - Article

VL - 15

SP - 7527

EP - 7532

JO - Organic and Biomolecular Chemistry

JF - Organic and Biomolecular Chemistry

SN - 1477-0520

ER -