Jessica M. L. Elwood
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Jessica M. L. Elwood has a total of 14 co-authors. Here are the top co-authors by number of shared publications:
- Craig Jamieson
Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, Glasgow, G1 1XL
2 shared publications J. Daniel Lopez-Fernandez
Department of Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, Glasgow G1 1XL, U.K.
2 shared publicationsKeith Livingstone
Department of Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, Glasgow G1 1XL, U.K.
2 shared publicationsMartyn C. Henry
Department of Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, Glasgow G1 1XL, U.K.
2 shared publicationsMhairi Boyle
Department of Pure and Applied Chemistry, University of Strathclyde, 295 Cathedral Street, Glasgow G1 1XL, U.K.
2 shared publications- Barbara Poniedziałek
Department of Environmental Medicine, Poznan University of Medical Sciences, 60-806 Poznan, Poland
1 shared publication
Latest Publications
- Open Access
- 16 December 2022
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 24 (51) , 9491-9496
Functionalized Tetrazoles as Latent Active Esters in the Synthesis of Amide Bonds
- 16 December 2022
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 24 (51) , 9491-9496
Open AccessFunctionalized Tetrazoles as Latent Active Esters in the Synthesis of Amide Bonds
- Open Access
- 29 December 2021
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 24 (1) , 334-338
Amide Bond Formation via the Rearrangement of Nitrile Imines Derived from N-2-Nitrophenyl Hydrazonyl Bromides
We report how the rearrangement of highly reactive nitrile imines derived from N-2-nitrophenyl hydrazonyl bromides can be harnessed for the facile construction of amide bonds. This amidation reaction was found to be widely applicable to the synthesis of primary, secondary, and tertiary amides and was used as the key step in the synthesis of the lipid-lowering agent bezafibrate. The orthogonality and functional group tolerance of this approach was exemplified by the N-acylation of unprotected amino acids.
- 29 December 2021
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 24 (1) , 334-338
Open AccessAmide Bond Formation via the Rearrangement of Nitrile Imines Derived from N-2-Nitrophenyl Hydrazonyl Bromides
We report how the rearrangement of highly reactive nitrile imines derived from N-2-nitrophenyl hydrazonyl bromides can be harnessed for the facile construction of amide bonds. This amidation reaction was found to be widely applicable to the synthesis of primary, secondary, and tertiary amides and was used as the key step in the synthesis of the lipid-lowering agent bezafibrate. The orthogonality and functional group tolerance of this approach was exemplified by the N-acylation of unprotected amino acids.
- Open Access
- 1 October 2017
- Published by Elsevier in Toxicology in Vitro
- Vol. 44, 172-181
Synthetic analogues of cyanobacterial alkaloid cylindrospermopsin and their toxicological activity
- 1 October 2017
- Published by Elsevier in Toxicology in Vitro
- Vol. 44, 172-181
Open AccessSynthetic analogues of cyanobacterial alkaloid cylindrospermopsin and their toxicological activity