William A. Maio
Affiliations: | Chemistry | New Mexico State University, Las Cruces, NM, United States |
Area:
Synthetic ChemistryWebsite:
http://www.williammaio.comGoogle:
"William Maio"Parents
Sign in to add mentor| Gary Herbert Posner | grad student | 2003-2008 | Johns Hopkins Medical School |
| Amos B. Smith, III | post-doc | 2008-2010 | Penn |
Children
Sign in to add trainee| Alexandra Elizabeth Golliher | grad student | 2017-2021 | New Mexico State University, Las Cruces |
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Publications
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| Bailey SJ, Sapkota RR, Golliher AE, et al. (2018) Lewis-Acid-Mediated Union of Epoxy-Carvone Diastereomers with Anisole Derivatives: Mechanistic Insight and Application to the Synthesis of Non-natural CBD Analogues. Organic Letters |
| Ai Y, Kozytska MV, Zou Y, et al. (2018) Total Synthesis of the Marine Phosphomacrolide, (-)-Enigmazole A, Exploiting Multicomponent Type I Anion Relay Chemistry (ARC) in Conjunction with a Late-Stage Petasis-Ferrier Union/Rearrangement. The Journal of Organic Chemistry |
| Posner GH, Hatcher MA, Maio WA. (2016) Copper and silicon mediated, HMPA-free, n+3 ring expansions for the construction of medium sized lactones and lactams: short synthesis of (+)-cis-lauthisan Tetrahedron. 72: 6025-6030 |
| Genna DT, Maio WA. (2016) There and back again: the synthetic travels of Gary H. Posner Tetrahedron. 72: 5956-5967 |
| DeGruyter JN, Maio WA. (2014) The taumycin A macrocycle: Asymmetric total synthesis and revision of relative stereochemistry Organic Letters. 16: 5196-5199 |
| Tello-Aburto R, Newar TD, Maio WA. (2012) Evolution of a protecting-group-free total synthesis: Studies en route to the neuroactive marine macrolide (-)-palmyrolide A Journal of Organic Chemistry. 77: 6271-6289 |
| Tello-Aburto R, Johnson EM, Valdez CK, et al. (2012) Asymmetric total synthesis and absolute stereochemistry of the neuroactive marine macrolide palmyrolide A. Organic Letters. 14: 2150-3 |
| Smith AB, Tong R, Kim WS, et al. (2011) Anion relay chemistry: Access to the type II ARC reaction manifold through a fundamentally different reaction pathway exploiting 1-oxa-2-silacyclopentanes and related congeners Angewandte Chemie - International Edition. 50: 8904-8907 |
| Posner GH, Maio WA, Kalinda AS. (2008) Electronically stabilized versions of the antimalarial acetal trioxanes artemether and artesunate Bioorganic and Medicinal Chemistry. 16: 5247-5253 |
| Posner GH, Chang W, Hess L, et al. (2008) Malaria-infected mice are cured by oral administration of new artemisinin derivatives. Journal of Medicinal Chemistry. 51: 1035-42 |