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N-(Diazoacetyl)oxazolidin-2-thiones as Sulfur-Donor Reagents: Asymmetric Synthesis of Thiiranes from Aldehydes.
- Published in:
- Angewandte Chemie International Edition, 2012, v. 51, n. 43, p. 10856, doi. 10.1002/anie.201204771
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- Article
Catalytic Enantioselective Synthesis of Tertiary Thiols From 5 H-Thiazol-4-ones and Nitroolefins: Bifunctional Ureidopeptide-Based Brønsted Base Catalysis.
- Published in:
- Angewandte Chemie International Edition, 2013, v. 52, n. 45, p. 11846, doi. 10.1002/anie.201305644
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- Article
Catalytic Enantioselective Synthesis of Tertiary Thiols From 5 H-Thiazol-4-ones and Nitroolefins: Bifunctional Ureidopeptide-Based Brønsted Base Catalysis.
- Published in:
- Angewandte Chemie, 2013, v. 125, n. 45, p. 12062, doi. 10.1002/ange.201305644
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- Publication type:
- Article
N-(Diazoacetyl)oxazolidin-2-thiones as Sulfur-Donor Reagents: Asymmetric Synthesis of Thiiranes from Aldehydes.
- Published in:
- Angewandte Chemie, 2012, v. 124, n. 43, p. 11014, doi. 10.1002/ange.201204771
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- Publication type:
- Article
α‐Hydroxy Ketones as Masked Ester Donors in Brønsted Base Catalyzed Conjugate Additions to Nitroalkenes.
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- Chemistry - A European Journal, 2018, v. 24, n. 15, p. 3893, doi. 10.1002/chem.201705968
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- Article
β<sup>2, 2</sup>-Amino Acid N-Carboxyanhydrides Relying on Sequential Enantioselective C(4)-Functionalization of Pyrrolidin-2,3-diones and Regioselective Baeyer-Villiger Oxidation.
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- Chemistry - A European Journal, 2017, v. 23, n. 34, p. 8185, doi. 10.1002/chem.201700464
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- Article
Frontispiece: β<sup>2, 2</sup>-Amino Acid N-Carboxyanhydrides Relying on Sequential Enantioselective C(4)-Functionalization of Pyrrolidin-2,3-diones and Regioselective Baeyer-Villiger Oxidation.
- Published in:
- Chemistry - A European Journal, 2017, v. 23, n. 34, p. n/a, doi. 10.1002/chem.201700464
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- Article
Diastereoselective ZnCl 2 -Mediated Joullié–Ugi Three-Component Reaction for the Preparation of Phosphorylated N -Acylaziridines from 2 H -Azirines.
- Published in:
- Molecules, 2024, v. 29, n. 5, p. 1023, doi. 10.3390/molecules29051023
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- Article