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Sign in to add mentor| Thomas R.R. Pettus | grad student | 2003-2008 | UC Santa Barbara | |
| (Diasteroselective Reactions of Cyclohexa-2,5-dienones, Building Blocks for Illudins, and the Synthesis of Berkelic Acid.) | ||||
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Publications
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| Guney T, Wenderski TA, Boudreau MW, et al. (2018) Synthesis of Benzannulated Medium-ring Lactams via a Tandem Oxidative Dearomatization-Ring Expansion Reaction. Chemistry (Weinheim An Der Bergstrasse, Germany) |
| Guney T, Wenderski TA, Boudreau MW, et al. (2018) Front Cover: Synthesis of Benzannulated Medium-ring Lactams via a Tandem Oxidative Dearomatization-Ring Expansion Reaction (Chem. Eur. J. 50/2018) Chemistry - a European Journal. 24: 13059-13059 |
| Bauer RA, Wenderski TA, Tan DS. (2013) Biomimetic diversity-oriented synthesis of benzannulated medium rings via ring expansion. Nature Chemical Biology. 9: 21-9 |
| Wenderski TA, Marsini MA, Pettus TR. (2011) A diastereoselective formal synthesis of berkelic acid. Organic Letters. 13: 118-21 |
| Wenderski TA, Hoarau C, Mejorado L, et al. (2010) Dearomatization applications of I((III)) reagents and some unusual reactivity amongst resorcinol derived cyclohexadienones. Tetrahedron. 66: 5873-5883 |
| Wenderski TA, Hoarau C, Mejorado L, et al. (2010) Dearomatization applications of I(III) reagents and some unusual reactivity amongst resorcinol derived cyclohexadienones Tetrahedron. 66: 5873-5883 |
| Wenderski TA, Denatale V, Pettus TR. (2009) Synthesis of 2,2-Disubstituted Pentalenes and Indenes by a Useful Modification to Nakamura's DMCP [3+2]-Cycloaddition Protocol. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 16: 2637-2642 |
| Wenderski TA, Huang S, Pettus TR. (2009) Enantioselective total synthesis of all of the known chiral cleroindicins (C-F): clarification among optical rotations and assignments. The Journal of Organic Chemistry. 74: 4104-9 |
| Pettus T, Wenderski T. (2008) Chapter 13 Seduced by a siren's call: expanding applications for aromatic compounds and the synthesis of (+)-rishirilide B Strategies and Tactics in Organic Synthesis. 7: 460-490 |