Paul Ronald Hanson

Affiliations: 
Chemistry University of Kansas, Lawrence, KS, United States 
Area:
Organic Synthesis
Website:
https://chemistry.drupal.ku.edu/people/faculty/phanson
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"Paul Hanson"
Bio:

http://www2.ku.edu/~chem/groups/hanson_grp/index.shtml

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Publications

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Dissanayake GC, Ndi CN, Markley JL, et al. (2023) Total Synthesis of Sanctolide A and Formal Synthesis of (2)-Sanctolide A. The Journal of Organic Chemistry. 88: 805-817
Javed S, Ganguly A, Dissanayake GC, et al. (2022) An Iterative Phosphate Tether Mediated Approach for the Synthesis of Complex Polyol Subunits. Organic Letters. 24: 16-21
Markley JL, Hanson PR. (2017) P-Tether-Mediated, Iterative SN2'-Cuprate Alkylation Strategy to Skipped Polyol Stereotetrads: Utility of an Oxidative "Function Switch" with Phosphite-Borane Tethers. Organic Letters
Markley JL, Hanson PR. (2017) P-Stereogenic Bicyclo[4.3.1]phosphite Boranes: Synthesis and Utility of Tunable P-Tether Systems for the Desymmetrization of C2-Symmetric 1,3-anti-Diols. Organic Letters
Faisal S, Zang Q, Maity PK, et al. (2017) Development and Application of a Recyclable High-Load Magnetic Co/C Hybrid ROMP-Derived Benzenesulfonyl Chloride Reagent and Utility of Corresponding Analogues. Organic Letters
Faisal S, Maity PK, Zang Q, et al. (2016) Synthesis of High-Load, Hybrid Silica-Immobilized Heterocyclic Benzyl Phosphate (Si-OHBP) and Triazolyl Phosphate (Si-OHTP) Alkylating Reagents. Acs Combinatorial Science
Faisal S, Maity PK, Zang Q, et al. (2016) Application of Silica-Supported Alkylating Reagents in a One-Pot, Sequential Protocol to Diverse Benzoxathiazepine 1,1-Dioxides. Acs Combinatorial Science
Maitra S, Bodugam M, Javed S, et al. (2016) Synthesis of the C9-C25 Subunit of Spirastrellolide B. Organic Letters
Javed S, Bodugam M, Torres J, et al. (2016) Modular Synthesis of Novel Macrocycles Bearing α,β-Unsaturated Chemotypes through a Series of One-Pot, Sequential Protocols. Chemistry (Weinheim An Der Bergstrasse, Germany)
Markley JL, Maitra S, Hanson PR. (2016) Phosphate Tether-Mediated Ring-Closing Metathesis for the Generation of P-Stereogenic, Z-Configured Bicyclo[7.3.1]- and Bicyclo[8.3.1]phosphates. The Journal of Organic Chemistry
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