Adrian L. Schwan, Ph.D.

Affiliations: 
Chemistry University of Guelph, Guelph, Ontario, Canada 
Area:
organosulfur chemistry
Website:
http://www.chemistry.uoguelph.ca/schwan/schwan.html
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"Adrian Schwan"
Bio:

Professor and Chair

Mean distance: 8.04
 
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Publications

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Nicol EA, Sing M, Luu LU, et al. (2023) The Synthesis and Base-Induced Breakdown of Triaryl 1,4-Oxathiins-An Experimental and DFT Study. Molecules (Basel, Switzerland). 28
Allen MA, Volosheniuk M, Nicol EA, et al. (2023) Cope-Type Hydroamination of Vinylboronates. Organic Letters. 25: 3045-3048
Schwan AL, Michalski MM, Findlay JP. (2019) Origins and applications of stereoselective sulfenate anion alkylation reactions Phosphorus Sulfur and Silicon and the Related Elements. 194: 692-697
Foy HC, Schwan AL, Dudding T. (2019) A mechanistic study of oxygen atom transfer from N-sulfonyloxaziridine to enolates Tetrahedron. 75: 2056-2061
Aitken RA, Hauduc C, Hossain MS, et al. (2014) Unexpected pyrolytic behaviour of substituted benzo[c]thiopyran and thieno[2,3-c]thiopyran s,s-dioxides Australian Journal of Chemistry. 67: 1288-1295
Söderman SC, Schwan AL. (2013) Stereodivergent access to cis- and trans-3,5-disubstituted 1,4-thiazane 1-oxides by cyclization of homochiral β-amino sulfoxides and sulfones. The preparation of isomeric ant venom alkaloids. Organic Letters. 15: 4434-7
Söderman SC, Schwan AL. (2013) Sulfenate substitution as a complement and alternative to sulfoxidation in the diastereoselective preparation of chiral β-substituted β-amino sulfoxides. The Journal of Organic Chemistry. 78: 1638-49
Ho LU, Shkoor MG, Hossain MS, et al. (2013) The base-mediated cyclization of selected benzyl alkynyl sulfones with aromatic aldehydes: Novel synthetic access to aryl-substituted 5,6-dihydro-1,4-oxathiin S,S -dioxides Journal of Sulfur Chemistry. 34: 79-87
Schwan AL, Söderman SC. (2013) Discoveries in sulfenic acid anion chemistry Phosphorus, Sulfur and Silicon and the Related Elements. 188: 275-286
Söderman SC, Schwan AL. (2012) 1,2-Dibromotetrachloroethane: an ozone-friendly reagent for the in situ Ramberg-Bäcklund rearrangement and its use in the formal synthesis of E-resveratrol. The Journal of Organic Chemistry. 77: 10978-84
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