Heather M. Sklenicka, Ph.D.

Affiliations: 
Chemistry Rochester Comm & Tech College 
Area:
Chemical Education
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"Heather Sklenicka"
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Richard P. Hsung grad student 1998-2003 UMN
 (Synthesis of decahydroquinoline containing natural products.)
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Publications

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Zehnder LR, Wei L, Hsung RP, et al. (2010) ChemInform Abstract: Stereoselective trans- and cis-Dihydroxylations of 2H-Pyranyl and Dihydropyridinyl Heterocycles Synthesized from Formal [3 + 3]-Cycloaddition Reactions of α,β-Unsaturated Iminium Ions with 1,3-Dicarbonyl Equivalents. Cheminform. 32: no-no
Li G, Carlson LJ, Sagamanova IK, et al. (2009) A Stereodivergent Approach for Accessing Both C2,8a-Syn and C2,8a-Anti Relative Stereochemical Manifolds in the Lepadin Family via a TiCL(4)-Promoted Aza-[3 + 3] Annulation. Synthesis. 2009: 2905
Ghosh SK, Buchanan GS, Long QA, et al. (2008) Aza- and Carbo-[3 + 3] Annulations of Exo-Cyclic Vinylogous Amides and Urethanes. Synthesis of Tetrahydroindolizidines and An Unexpected Formation of Hexahydroquinolines. Tetrahedron. 64: 883-893
Shen HC, Wang J, Cole KP, et al. (2003) A formal [3 + 3] cycloaddition reaction. Improved reactivity using alpha,beta-unsaturated iminium salts and evidence for reversibility of 6pi-electron electrocyclic ring closure of 1-oxatrienes. The Journal of Organic Chemistry. 68: 1729-35
Hsung RP, Wei L, Sklenicka HM, et al. (2003) A Formal [3 + 3] Cycloaddition Strategy for the Synthesis of Heterocycles Cheminform. 34
Sklenicka HM, Hsung RP, McLaughlin MJ, et al. (2002) Stereoselective formal [3 + 3] cycloaddition approach to cis-1-azadecalins and synthesis of (-)-4a,8a-diepi-pumiliotoxin C. evidence for the first highly stereoselective 6pi-electron electrocyclic ring closures of 1-azatrienes. Journal of the American Chemical Society. 124: 10435-42
Sklenicka HM, Hsung RP. (2002) Recent approaches to cis-azadecalins: Synthesis of dendrobatid alkaloid pumiliotoxin C Chemtracts. 15: 391-401
Wei LL, Hsung RP, Sklenicka HM, et al. (2001) A Novel and Highly Stereoselective Intramolecular Formal [3+3] Cycloaddition Reaction of Vinylogous Amides Tethered with α,β-Unsaturated Aldehydes: A Formal Total Synthesis of (+)-Gephyrotoxin. Angewandte Chemie (International Ed. in English). 40: 1516-1518
Zehnder LR, Wei LL, Hsung RP, et al. (2001) Stereoselective trans- and cis-dihydroxylations of 2H-pyranyl and dihydropyridinyl heterocycles synthesized from formal [3 + 3]-cycloaddition reactions of alpha,beta-unsaturated iminium ions with 1,3-dicarbonyl equivalents. Organic Letters. 3: 2141-4
Wei LL, Hsung RP, Sklenicka HM, et al. (2001) A Novel and Highly Stereoselective Intramolecular Formal Angewandte Chemie (International Ed. in English). 40: 1516-1518
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