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Paul S. Tanis

Observed names: P. S. Tanis, Tanis, P.S., Tanis, Paul S.
Institution: Columbia University
OpenAlex ID: A5045027502
Identification of an unexpected 2-oxonia[3,3]sigmatropic rearrangement/aldol pathway in the formation of oxacyclic rings. Total synthesis of (+)-aspergillin PZ
2011 · Stephen M. Canham, Larry E. Overman, et al. · Tetrahedron · 45
Origin of Stereocontrol in the Construction of the 12-Oxatricyclo[6.3.1.02,7]dodecane Ring System by Prins−Pinacol Reactions
2009 · Larry E. Overman, Paul S. Tanis · The Journal of Organic Chemistry · 22
Exploiting Pseudo C2-Symmetry for an Efficient Synthesis of the F-Ring of the Spongistatins
2013 · Paul S. Tanis, Joshua R. Infantine, et al. · Organic Letters · 11
Design and 22-step synthesis of highly potent D-ring modified and linker-equipped analogs of spongistatin 1
2018 · Linda M. Suen, Makeda A. Tekle-Smith, et al. · Nature Communications · 8
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Design, 22-step synthesis, and evaluation of highly potent D-ring modified and linker-equipped analogs of spongistatin 1
2018 · James Leighton, Linda M. Suen, et al. · ChemRxiv
CCDC 833185: Experimental Crystal Structure Determination
2017 · Canham, S.M., Overman, L.E., et al. · The Cambridge Structural Database
ChemInform Abstract: Exploiting Pseudo C2‐Symmetry for an Efficient Synthesis of the F‐Ring of the Spongistatins.
2014 · Paul S. Tanis, Joshua R. Infantine, et al. · ChemInform
CCDC 970609: Experimental Crystal Structure Determination
2013 · Tanis, Paul S., Infantine, Joshua R., et al. · The Cambridge Structural Database
CCDC 833184: Experimental Crystal Structure Determination
2012 · Canham, S.M., Overman, L.E., et al. · The Cambridge Structural Database
CCDC 753122: Experimental Crystal Structure Determination
2011 · Overman, L.E., Tanis, P.S. · The Cambridge Structural Database
Stereochemistry of the Prins-Pinacol Rearrangement
2010 · L. E. Overman, P. S. Tanis · Synfacts
Works count: 11
Citation count: 86
H-index: 4
I10-index: 3
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