Found: 22
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Stereodivergent Synthesis of Spiroaminals via Chiral Bifunctional Hydrogen Bonding Organocatalysis.
- Published in:
- Angewandte Chemie, 2024, v. 136, n. 22, p. 1, doi. 10.1002/ange.202404106
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- Article
Stereodivergent Synthesis of Spiroaminals via Chiral Bifunctional Hydrogen Bonding Organocatalysis.
- Published in:
- Angewandte Chemie International Edition, 2024, v. 63, n. 22, p. 1, doi. 10.1002/anie.202404106
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- Article
An Organocatalytic Highly Enantioselective Stereospecific Synthesis of 1,1‐Disubstituted‐1,3‐Dihydroisobenzofurans.
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- Chemistry - A European Journal, 2024, v. 30, n. 25, p. 1, doi. 10.1002/chem.202303980
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- Article
Organocatalytic Enantioselective Intramolecular Michael Addition by In Situ Generated Aminoisobenzofulvenes: Construction of Spiro Quaternary Carbon Stereocenters.
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- Chemistry - A European Journal, 2023, v. 29, n. 59, p. 1, doi. 10.1002/chem.202301563
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- Article
Expedient Access to Enantioenriched 1‐Azaspiro Cyclobutanones Enabled by Modified Heyns Rearrangement.
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- Angewandte Chemie, 2023, v. 135, n. 32, p. 1, doi. 10.1002/ange.202306179
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- Article
Expedient Access to Enantioenriched 1‐Azaspiro Cyclobutanones Enabled by Modified Heyns Rearrangement.
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- Angewandte Chemie International Edition, 2023, v. 62, n. 32, p. 1, doi. 10.1002/anie.202306179
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- Article
Organocatalytic Desymmetric Conjugate Addition to Cyclobutanone: An Enantio‐ and Diastereoselective Synthesis of [6,5,4]‐Fused Carbocycles.
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- Chemistry - A European Journal, 2023, v. 29, n. 24, p. 1, doi. 10.1002/chem.202203407
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- Article
Chiral Amine Catalyzed Reductive Aldol/Reductive Michael Addition Cascade Towards Enantioselective Synthesis of Benzannulated Diquinanes.
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- European Journal of Organic Chemistry, 2023, v. 26, n. 14, p. 1, doi. 10.1002/ejoc.202201409
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- Article
Cinchonamine Squaramide Catalyzed Asymmetric aza‐Michael Reaction: Dihydroisoquinolines and Tetrahydropyridines.
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- Angewandte Chemie, 2018, v. 130, n. 30, p. 9541, doi. 10.1002/ange.201805020
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- Article
Cinchonamine Squaramide Catalyzed Asymmetric aza‐Michael Reaction: Dihydroisoquinolines and Tetrahydropyridines.
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- Angewandte Chemie International Edition, 2018, v. 57, n. 30, p. 9397, doi. 10.1002/anie.201805020
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- Article
Dynamic Kinetic Spiroketalization/Oxa-Michael Addition Cascade of Alkoxyboronates and Peroxyacetals: Enantio- and Diastereoselective Synthesis of Benzannulated Spiroketals.
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- Chemistry - A European Journal, 2017, v. 23, n. 47, p. 11216, doi. 10.1002/chem.201701291
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- Article
Organocatalytic, Enantioselective Synthesis of Cyclohexadienone Containing Hindered Spirocyclic Ethers through an Oxidative Dearomatization/Oxa-Michael Addition Sequence.
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- Angewandte Chemie, 2016, v. 128, n. 48, p. 15339, doi. 10.1002/ange.201607039
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- Article
Organocatalytic, Enantioselective Synthesis of Cyclohexadienone Containing Hindered Spirocyclic Ethers through an Oxidative Dearomatization/Oxa-Michael Addition Sequence.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 48, p. 15115, doi. 10.1002/anie.201607039
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- Article
Enantio- and Diastereoselective Synthesis of exo-Peroxyacetals: An Organocatalyzed Peroxyhemiacetalization/oxa-Michael Addition Cascade.
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- Angewandte Chemie, 2016, v. 128, n. 27, p. 7854, doi. 10.1002/ange.201511165
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- Article
Transition-Metal-Free Synthesis of Homo- and Hetero-1,2,4-Triaryl Benzenes by an Unexpected Base-Promoted Dearylative Pathway.
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- Angewandte Chemie, 2016, v. 128, n. 27, p. 7859, doi. 10.1002/ange.201511424
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- Article
Enantio- and Diastereoselective Synthesis of exo-Peroxyacetals: An Organocatalyzed Peroxyhemiacetalization/oxa-Michael Addition Cascade.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 27, p. 7723, doi. 10.1002/anie.201511165
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- Article
Transition-Metal-Free Synthesis of Homo- and Hetero-1,2,4-Triaryl Benzenes by an Unexpected Base-Promoted Dearylative Pathway.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 27, p. 7728, doi. 10.1002/anie.201511424
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- Article
Palladium-Catalyzed Oxidative Cycloisomerization of 2-Cinnamyl-1,3-Dicarbonyls: Synthesis of Functionalized 2-Benzyl Furans.
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- Chemistry - A European Journal, 2015, v. 21, n. 42, p. 14732, doi. 10.1002/chem.201502781
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- Article
Synthesis of Air- and Moisture-Stable, Storable Chiral Oxorhenium Complexes and Their Application as Catalysts for the Enantioselective Imine Reduction.
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- Chemistry - A European Journal, 2015, v. 21, n. 36, p. 12601, doi. 10.1002/chem.201501914
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- Article
Inside Cover: Tritium-Labeled N<sup>1</sup>-[3-(1 H-imidazol-4-yl)propyl]- N<sup>2</sup>-propionylguanidine ([<sup>3</sup>H]UR-PI294), a High-Affinity Histamine H<sub>3</sub> and H<sub>4</sub> Receptor Radioligand / N<sup>G</sup>-Acylated Aminothiazolylpropylguanidines as Potent and Selective Histamine H<sub>2</sub> Receptor Agonists (ChemMedChem 2/2009)
- Published in:
- ChemMedChem, 2009, v. 4, n. 2, p. 134, doi. 10.1002/cmdc.200990005
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- Article
N<sup>G</sup>-Acylated Aminothiazolylpropylguanidines as Potent and Selective Histamine H<sub>2</sub> Receptor Agonists.
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- ChemMedChem, 2009, v. 4, n. 2, p. 232, doi. 10.1002/cmdc.200800296
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- Article
Point mutations in the second extracellular loop of the histamine H<sub>2</sub> receptor do not affect the species-selective activity of guanidine-type agonists.
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- Naunyn-Schmiedeberg's Archives of Pharmacology, 2007, v. 376, n. 4, p. 253, doi. 10.1007/s00210-007-0204-4
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- Article