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Organocatalytic Strategy for the Enantioselective Cycloaddition to Trisubstituted Nitroolefins to Create Spirocyclohexene-Oxetane Scaffolds.
- Published in:
- Angewandte Chemie International Edition, 2016, v. 55, n. 7, p. 2478, doi. 10.1002/anie.201510731
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Organocatalytic Strategy for the Enantioselective Cycloaddition to Trisubstituted Nitroolefins to Create Spirocyclohexene-Oxetane Scaffolds.
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- Angewandte Chemie, 2016, v. 128, n. 7, p. 2524, doi. 10.1002/ange.201510731
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- Article
Structure and Absolute Configuration of Kongiidiazadione, a New Phytotoxic 3-Substituted-5-Diazenylcyclopentendione Produced by Diaporthe Kongii.
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- Chirality, 2015, v. 27, n. 9, p. 557, doi. 10.1002/chir.22466
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- Article
Cover Feature: Absolute Configuration Assignment from Optical Rotation Data by Means of Biphenyl Chiroptical Probes (Chem. Eur. J. 22/2019).
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- Chemistry - A European Journal, 2019, v. 25, n. 22, p. 5597, doi. 10.1002/chem.201901165
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Absolute Configuration Assignment from Optical Rotation Data by Means of Biphenyl Chiroptical Probes.
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- Chemistry - A European Journal, 2019, v. 25, n. 22, p. 5682, doi. 10.1002/chem.201806435
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- Article
Methylene C(sp<sup>3</sup>)−H Arylation Enables the Stereoselective Synthesis and Structure Revision of Indidene Natural Products.
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- Angewandte Chemie, 2024, v. 136, n. 1, p. 1, doi. 10.1002/ange.202316103
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- Article
Methylene C(sp<sup>3</sup>)−H Arylation Enables the Stereoselective Synthesis and Structure Revision of Indidene Natural Products.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 1, p. 1, doi. 10.1002/anie.202316103
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- Article
Absolute Configuration Sensing of Chiral Aryl- and Aryloxy-Propionic Acids by Biphenyl Chiroptical Probes.
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- Chemosensors, 2021, v. 9, n. 7, p. 154, doi. 10.3390/chemosensors9070154
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