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Recent Syntheses and Strategies toward Polycyclic Gelsemium Alkaloids.
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- Angewandte Chemie, 2019, v. 131, n. 3, p. 692, doi. 10.1002/ange.201807509
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- Article
Enantioselective Synthesis of (−)‐Halenaquinone.
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- Angewandte Chemie, 2018, v. 130, n. 29, p. 9255, doi. 10.1002/ange.201805370
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- Article
Schinortriterpenoide: eine Fallstudie in Synthesedesign.
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- Angewandte Chemie, 2017, v. 129, n. 7, p. 1728, doi. 10.1002/ange.201609372
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- Article
Recent Syntheses and Strategies toward Polycyclic Gelsemium Alkaloids.
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- Angewandte Chemie International Edition, 2019, v. 58, n. 3, p. 681, doi. 10.1002/anie.201807509
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- Article
Enantioselective Synthesis of (−)‐Halenaquinone.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 29, p. 9117, doi. 10.1002/anie.201805370
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- Article
Schinortriterpenoids: A Case Study in Synthetic Design.
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- Angewandte Chemie International Edition, 2017, v. 56, n. 7, p. 1704, doi. 10.1002/anie.201609372
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- Article
Correction: Innovation and Entrepreneurship in Promotion and Tenure in Biomedical Engineering.
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- 2023
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- Correction Notice
Innovation and Entrepreneurship in Promotion and Tenure in Biomedical Engineering: Communication from the Biomedical Engineering Society Long Range Planning Committee.
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- Cellular & Molecular Bioengineering, 2023, v. 16, n. 3, p. 181, doi. 10.1007/s12195-023-00767-x
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- Article
Enantioselective Total Synthesis of Amphidinolide F.
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- Angewandte Chemie, 2012, v. 124, n. 32, p. 8072, doi. 10.1002/ange.201203935
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- Article
Titelbild: Enantioselective Total Synthesis of Amphidinolide F (Angew. Chem. 32/2012).
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- Angewandte Chemie, 2012, v. 124, n. 32, p. 7985, doi. 10.1002/ange.201205172
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- Article
Front Cover: Asymmetric Construction of Vicinal Stereocenters Containing Quaternary and Tertiary Carbons: Application to the Formal Synthesis of (–)‐Chenopodene (Eur. J. Org. Chem. 4/2020).
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 4, p. 406, doi. 10.1002/ejoc.202000090
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- Article
Asymmetric Construction of Vicinal Stereocenters Containing Quaternary and Tertiary Carbons: Application to the Formal Synthesis of (–)‐Chenopodene.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 4, p. 420, doi. 10.1002/ejoc.201901722
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- Article
Diels–Alder Approach to Polysubstituted Biaryls: Rapid Entry to Tri- and Tetra-ortho-substituted Phosphorus-Containing BiarylsFinancial support was provided by the National Science Foundation (CHE-0549884). The authors would also like to thank Professor Max Deinzer (OSU) and Dr. Jeff Morré (OSU) for mass-spectral data, Dr. Lev Zakharov (OSU) for the X-ray crystallographic analysis of 14, and Dr. Roger Hanselmann (Rib-X Pharmaceuticals) for his helpful discussions.
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- Angewandte Chemie, 2006, v. 118, n. 40, p. 6889, doi. 10.1002/ange.200602683
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- Article
Proline Sulfonamide-Catalyzed, Domino Process for Asymmetric Synthesis of Amino- and Hydroxy-Substituted Bicyclo[2.2.2]octanes.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 1, p. 150, doi. 10.1002/ejoc.201501302
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- Article
Highly Enantioselective Construction of Polycyclic Spirooxindoles by Organocatalytic 1,3-Dipolar Cycloaddition of 2-Cyclohexenone Catalyzed by Proline-Sulfonamide.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 26, p. 5700, doi. 10.1002/ejoc.201402953
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- Article
Synthesis of the Southern FGHI Ring System of Azaspiracid-1 and Investigation into the Controlling Elements of C28- and C36-Ketalization.
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- Angewandte Chemie International Edition, 2007, v. 46, n. 7, p. 1004, doi. 10.1002/anie.200790017
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- Article
Synthesis of the Southern FGHI Ring System of Azaspiracid-1 and Investigation into the Controlling Elements of C28- and C36-Ketalization.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 45, p. 7622, doi. 10.1002/anie.200603353
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- Publication type:
- Article
Diels–Alder Approach to Polysubstituted Biaryls: Rapid Entry to Tri- and Tetra-ortho-substituted Phosphorus-Containing BiarylsFinancial support was provided by the National Science Foundation (CHE-0549884). The authors would also like to thank Professor Max Deinzer (OSU) and Dr. Jeff Morré (OSU) for mass-spectral data, Dr. Lev Zakharov (OSU) for the X-ray crystallographic analysis of 14, and Dr. Roger Hanselmann (Rib-X Pharmaceuticals) for his helpful discussions.
- Published in:
- Angewandte Chemie International Edition, 2006, v. 45, n. 40, p. 6737, doi. 10.1002/anie.200602683
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- Publication type:
- Article
Synthesis of the C1-C26 Northern Portion of Azaspiracid-1: Kinetic versus Thermodynamic Control of the Formation of the Bis-spiroketal.
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- Angewandte Chemie International Edition, 2006, v. 45, n. 11, p. 1787, doi. 10.1002/anie.200503733
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- Article
Synthetic strategy: Moving backwards in new ways.
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- Nature Chemistry, 2010, v. 2, n. 8, p. 613, doi. 10.1038/nchem.758
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- Article
Enantioselective Total Synthesis of Amphidinolide F.
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- Angewandte Chemie International Edition, 2012, v. 51, n. 32, p. 7948, doi. 10.1002/anie.201203935
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- Article
Cover Picture: Enantioselective Total Synthesis of Amphidinolide F (Angew. Chem. Int. Ed. 32/2012).
- Published in:
- Angewandte Chemie International Edition, 2012, v. 51, n. 32, p. 7863, doi. 10.1002/anie.201205172
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- Article