Ashley M. Adams

ORCID: 0000-0003-0823-3709
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About
Contact & Profiles
Research Areas
  • Synthesis and Catalytic Reactions
  • Catalytic C–H Functionalization Methods
  • Click Chemistry and Applications
  • Metal-Catalyzed Oxygenation Mechanisms
  • Chemical Synthesis and Analysis
  • Oxidative Organic Chemistry Reactions
  • Multicomponent Synthesis of Heterocycles
  • Synthesis and Biological Evaluation
  • Computational Drug Discovery Methods
  • Complementary and Alternative Medicine Studies
  • Genetics, Bioinformatics, and Biomedical Research
  • Biotin and Related Studies
  • Chemical Synthesis and Reactions
  • Antibiotic Use and Resistance
  • Pharmaceutical Practices and Patient Outcomes
  • Iron Metabolism and Disorders
  • Mesoporous Materials and Catalysis
  • Cancer Treatment and Pharmacology
  • Viral Infections and Immunology Research
  • Food Security and Health in Diverse Populations
  • Supercapacitor Materials and Fabrication
  • Machine Learning in Materials Science
  • Microtubule and mitosis dynamics
  • X-ray Diffraction in Crystallography
  • Carbohydrate Chemistry and Synthesis

Arrien Pharmaceuticals (United States)
2025

Recursion (United States)
2025

South College
2022-2024

Exscien (United States)
2023

GlaxoSmithKline (United States)
2022

University of Illinois Urbana-Champaign
2022

Stanford University
2013-2018

Discovery Institute
2016

Cornell University
2008-2012

Selective hydroxylation of 3° and benzylic C–H bonds is made possible using a non-metal-based catalyst system, Oxone as the terminal oxidant, an aqueous fluoroalcohol solvent mixture. The choice uniquely effective for this process, but seemingly at odds with our finding that H2O promotes reduction oxaziridine intermediate. Our studies suggest reaction occurring within microdroplet, which both concentrates reactants mitigates deleterious impact on stability. These discoveries have led to...

10.1039/c3sc52649f article EN Chemical Science 2013-11-22

A comparative study is disclosed that seeks to highlight the current limitations and challenges exist in field of atom-transfer C–H oxidations. State-of-the-art methods are benchmarked order showcase clear differences similarities. novel Mn-mediated method for oxidation serves as a rapid simple aliphatic hydroxylation. Finally, two allow presence pyridine-containing substrates studied, something rare but great interest chemical community.

10.1021/acs.orglett.5b03047 article EN Organic Letters 2015-12-09

The desire for maximally efficient transformations in complex molecule synthesis has contributed to a surge of interest C–H functionalization methods development recent years. In contrast the steady stream methodological reports, however, there are noticeably fewer studies comparing efficacies different protocols on single structurally intricate substrate. Recognizing importance heteroatom incorporation synthesis, this report discloses comparative examination diverse strategies C–O, C–N, and...

10.1021/acs.joc.7b03291 article EN publisher-specific-oa The Journal of Organic Chemistry 2018-01-09

Using the Passerini and Ugi reactions as representative tests, utility of several α-substituted ketones R−CO−CH2−X (X = sulfonyloxy, acyloxy, azido, halo, hydroxy, sulfonyl) in isonitrile-based multicomponent was explored. In a relative rate study (R PhCH2CH2), each underwent condensation more rapidly than parent ketone. Short, highly convergent routes to oxazoline, β-lactam, di-O-acylglyceramides, other molecular frameworks were developed.

10.1021/jo8019708 article EN The Journal of Organic Chemistry 2008-10-22

Mechanistic insight into the C–H hydroxylation reaction catalysed by [(Me<sub>3</sub>tacn)RuCl<sub>3</sub>] has been obtained using desorption electrospray ionization mass spectrometry (DESI-MS) to identify reactive intermediates and determine fate of starting metal complex.

10.1039/c4sc01050g article EN Chemical Science 2014-01-01

In this Letter, we adapt a recently reported Pd-catalyzed transannular C(sp3)-H arylation of alicyclic amines for applications in fragment-based drug discovery (FBDD). We apply method to the synthesis series 6-arylated 3-azabicyclo[3.1.0]hexanes that are rule-of-three compliant fragments. Several modifications were made C-H enhance its utility fragment synthesis. These include use microwave heating shorten reaction times under 1 h and development new approaches directing group cleavage....

10.1055/s-0037-1610861 article EN cc-by-nd Synlett 2019-02-05

Abstract Background Violent crime (i.e., homicide, armed robbery, aggravated assault, and rape) continues to be a major public health concern in America. Several studies have linked the availability density of specific features retail food environment, such as convenience stores liquor stores, violent rates due criminal activity that often occurs near these retailers. Nevertheless, there limited understanding how other (e.g., grocery supercenters, restaurants, etc.) are associated with...

10.1186/s12889-022-14415-y article EN cc-by BMC Public Health 2022-11-01

Abstract A novel and rapid Mn‐mediated method for aliphatic C—H hydroxylation is described.

10.1002/chin.201618041 article EN ChemInform 2016-04-01

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at glance that was extracted from about 200 leading journals. To access of an article which published elsewhere, please select “Full Text” option. The original trackable via the “References”

10.1002/chin.200915053 article EN ChemInform 2009-03-23

Abstract ChemInform is a weekly Abstracting Service, delivering concise information at glance that was extracted from about 200 leading journals. To access of an article which published elsewhere, please select “Full Text” option. The original trackable via the “References”

10.1002/chin.200902058 article EN ChemInform 2008-12-12

ADVERTISEMENT RETURN TO ISSUEPREVIn This IssueNEXTIn Issue, Volume 10, Issue 7Ashley M. AdamsAshley AdamsMore by Ashley Adams and Terry W. MooreTerry MooreMore Moorehttp://orcid.org/0000-0002-5410-306XCite this: ACS Med. Chem. Lett. 2019, 7, 1015Publication Date (Web):July 11, 2019Publication History Published online11 July 2019Published inissue 11 2019https://pubs.acs.org/doi/10.1021/acsmedchemlett.9b00288https://doi.org/10.1021/acsmedchemlett.9b00288in-briefACS PublicationsCopyright © 2019...

10.1021/acsmedchemlett.9b00288 article EN other-oa ACS Medicinal Chemistry Letters 2019-07-11
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