☰ Chemistry Tree

Matthew H. Todd, Ph.D.

Affiliations:	2010		Stanford University, Palo Alto, CA
	2005-	Chemistry	University of Sydney, Camperdown, New South Wales, Australia

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Parents

Christopher Abell	grad student	1994-1999	Cambridge
Barry M. Trost	research scientist	2010-2010	Stanford

Children

Andrew J. Counsell	grad student	2014-2014	University of Sydney
Paul T. A. King	grad student	2016-2020	UCL
Alice Williamson	post-doc	2012-2015	University of Sydney

Collaborators

BETA: Related publications

Publications

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Tilley L, Xie S, Wang Y, et al. (2023) Reaction hijacking inhibition of Plasmodium falciparum asparagine tRNA synthetase. Research Square
Ball SR, Adamson JSP, Sullivan MA, et al. (2022) Perphenazine-Macrocycle Conjugates Rapidly Sequester the Aβ42 Monomer and Prevent Formation of Toxic Oligomers and Amyloid. Acs Chemical Neuroscience
Müller S, Ackloo S, Al Chawaf A, et al. (2021) Target 2035 - update on the quest for a probe for every protein. Rsc Medicinal Chemistry. 13: 13-21
Counsell AJ, Yu M, Shi M, et al. (2021) Copper(II) complexes of -propargyl cyclam ligands reveal a range of coordination modes and colours, and unexpected reactivity. Dalton Transactions (Cambridge, England : 2003)
Frei A, Zuegg J, Elliott AG, et al. (2020) Correction: Metal complexes as a promising source for new antibiotics. Chemical Science. 11: 4531
Korsik M, Tse E, Smith DG, et al. (2020) Tele-substitution Reactions in the Synthesis of a Promising Class of 1,2,4-Triazolo[4,3-a]pyrazine-Based Antimalarials. The Journal of Organic Chemistry
Tse E, Houston SD, Williams CM, et al. (2020) Non-Classical Phenyl Bioisosteres as Effective Replacements in a Series of Novel Open Source Antimalarials. Journal of Medicinal Chemistry
Frei A, Zuegg J, Elliott AG, et al. (2020) Metal complexes as a promising source for new antibiotics. Chemical Science. 11: 2627-2639
Frei A, Zuegg J, Elliott AG, et al. (2020) Correction: Metal complexes as a promising source for new antibiotics Chemical Science. 11: 4531-4531
Guardia A, Baiget J, Cacho M, et al. (2018) Easy-to-Synthesize Spirocyclic Compounds Possess Remarkable In Vivo Activity Against Mycobacterium Tuberculosis. Journal of Medicinal Chemistry

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