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A General Strategy for the Construction of Calyciphylline A‐Type Alkaloids: Divergent Total Syntheses of (−)‐Daphenylline and (−)‐Himalensine A.
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- Angewandte Chemie, 2021, v. 133, n. 17, p. 9525, doi. 10.1002/ange.202016212
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A Divergent Enantioselective Total Synthesis of Post‐Iboga Indole Alkaloids.
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- Angewandte Chemie, 2020, v. 132, n. 42, p. 18890, doi. 10.1002/ange.202008242
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- Article
Living Supramolecular Polymerization of an Aza‐BODIPY Dye Controlled by a Hydrogen‐Bond‐Accepting Triazole Unit Introduced by Click Chemistry.
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- Angewandte Chemie, 2020, v. 132, n. 13, p. 5223, doi. 10.1002/ange.201914966
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Regiodivergent Intramolecular Nucleophilic Addition of Ketimines for the Diverse Synthesis of Azacycles.
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- Angewandte Chemie, 2020, v. 132, n. 4, p. 1651, doi. 10.1002/ange.201910864
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Phosphite‐Catalyzed C−H Allylation of Azaarenes via an Enantioselective [2,3]‐Aza‐Wittig Rearrangement.
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- Angewandte Chemie, 2019, v. 131, n. 40, p. 14242, doi. 10.1002/ange.201906681
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Synthesis of Indolines and Derivatives by Aza‐Heck Cyclization.
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- Angewandte Chemie, 2019, v. 131, n. 38, p. 13582, doi. 10.1002/ange.201907758
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Enantioselective N‐Heterocyclic Carbene Catalysis that Exploits Imine Umpolung.
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- Angewandte Chemie, 2019, v. 131, n. 12, p. 4047, doi. 10.1002/ange.201812585
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Synthesis of N−H Bearing Imidazolidinones and Dihydroimidazolones Using Aza‐Heck Cyclizations.
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- Angewandte Chemie, 2018, v. 130, n. 37, p. 12257, doi. 10.1002/ange.201806295
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Catalytic Enantioselective Aza‐Benzoin Reactions of Aldehydes with 2<italic>H</italic>‐Azirines.
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- Angewandte Chemie, 2018, v. 130, n. 14, p. 3829, doi. 10.1002/ange.201712785
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Squaramide-Catalyzed Asymmetric aza-Friedel-Crafts/N,O-Acetalization Domino Reactions Between 2-Naphthols and Pyrazolinone Ketimines.
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- Angewandte Chemie, 2017, v. 129, n. 48, p. 15560, doi. 10.1002/ange.201709224
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Ring Expansion, Photoisomerization, and Retrocyclization of 1,4,2-Diazaboroles.
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- Angewandte Chemie, 2017, v. 129, n. 46, p. 14764, doi. 10.1002/ange.201708720
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Enantioselective Organocatalytic Intramolecular Aza-Diels-Alder Reaction.
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- Angewandte Chemie, 2017, v. 129, n. 35, p. 10709, doi. 10.1002/ange.201705746
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Practical Alkoxythiocarbonyl Auxiliaries for Iridium(I)-Catalyzed C−H Alkylation of Azacycles.
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- Angewandte Chemie, 2017, v. 129, n. 35, p. 10666, doi. 10.1002/ange.201704755
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Catalytic Enantioselective Aza-pinacol Rearrangement.
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- Angewandte Chemie, 2017, v. 129, n. 31, p. 9345, doi. 10.1002/ange.201705539
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Reversible Photothermal Isomerization of Carborane-Fused Azaborole to Borirane: Synthesis and Reactivity of Carbene-Stabilized Carborane-Fused Borirane.
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- Angewandte Chemie, 2017, v. 129, n. 31, p. 9326, doi. 10.1002/ange.201704642
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Innentitelbild: Enantioselective Aza-Ene-type Reactions of Enamides with Gold Carbenes Generated from α-Diazoesters (Angew. Chem. 12/2017).
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- Angewandte Chemie, 2017, v. 129, n. 12, p. 3158, doi. 10.1002/ange.201701298
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Enantioselective Aza-Ene-type Reactions of Enamides with Gold Carbenes Generated from α-Diazoesters.
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- Angewandte Chemie, 2017, v. 129, n. 12, p. 3295, doi. 10.1002/ange.201612208
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An Electron-Deficient Azacoronene Obtained by Radial π Extension.
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- Angewandte Chemie, 2016, v. 128, n. 47, p. 14878, doi. 10.1002/ange.201608400
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Donor-Stabilized 1,3-Disila-2,4-diazacyclobutadiene with a Nonbonded Si⋅⋅⋅Si Distance Compressed to a Si=Si Double Bond Length.
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- Angewandte Chemie, 2016, v. 128, n. 47, p. 14893, doi. 10.1002/ange.201608416
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Azaborabutadienes: Synthesis by Metal-Free Carboboration of Nitriles and Utility as Building Blocks for B,N-Heterocycles.
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- Angewandte Chemie, 2016, v. 128, n. 47, p. 14938, doi. 10.1002/ange.201608994
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Hydrogen Peroxide Solvates of 2,4,6,8,10,12-Hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane.
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- Angewandte Chemie, 2016, v. 128, n. 42, p. 13312, doi. 10.1002/ange.201607130
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Transition-Metal-Free Synthesis of N-Hydroxy Oxindoles by an Aza-Nazarov-Type Reaction Involving Azaoxyallyl Cations.
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- Angewandte Chemie, 2016, v. 128, n. 42, p. 13480, doi. 10.1002/ange.201607177
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A syn-Selective Aza-Aldol Reaction of Boron Aza-Enolates Generated from N-Sulfonyl-1,2,3-Triazoles and 9-BBN-H.
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- Angewandte Chemie, 2016, v. 128, n. 30, p. 8874, doi. 10.1002/ange.201603270
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BINOL Macrocycle Derivatives: Synthesis of New Dinaphthyl Sulfide Aza Oxa Thia Crowns (Lariats).
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- Journal of Chemistry, 2013, p. 1, doi. 10.1155/2013/598937
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An Efficient One-Pot Multicomponent Synthesis of 4-Aza-Podophyllotoxin Derivatives in Ionic Liquid.
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- Journal of Chemistry, 2013, p. 1, doi. 10.1155/2013/169695
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Polypyridines, Picrates, Lanthanides: A Plethora of Stacks?
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- Australian Journal of Chemistry, 2020, v. 73, n. 6, p. 529, doi. 10.1071/CH19367
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Cobalt‐Catalyzed Enantioselective Ring‐Opening Reactions of Oxa‐ and Aza‐bicyclic Alkenes with Alkenylboronic Acids.
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- Chinese Journal of Chemistry, 2022, v. 40, n. 2, p. 190, doi. 10.1002/cjoc.202100622
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Regioselective and Stereospecific Deuteration of Bioactive Aza Compounds by the Use of Ruthenium Nanoparticles.
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- Angewandte Chemie International Edition, 2014, v. 53, n. 1, p. 230, doi. 10.1002/anie.201307930
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Highly Enantioselective Aza-Diels-Alder Reaction of 1-Azadienes with Enecarbamates Catalyzed by Chiral Phosphoric Acids.
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- Angewandte Chemie International Edition, 2013, v. 52, n. 42, p. 11088, doi. 10.1002/anie.201304969
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Preparation and antiplasmodial activity of 3',4'‐dihydro‐1'H‐spiro(indoline‐3,2'‐quinolin)‐2‐ones.
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- Chemical Biology & Drug Design, 2019, v. 94, n. 4, p. 1849, doi. 10.1111/cbdd.13598
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Preparation of CL-20 Explosive Nanoparticles and Their Thermal Decomposition Property.
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- Journal of Nanomaterials, 2016, p. 1, doi. 10.1155/2016/5462097
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Molecular Rearrangement of an Aza-Scorpiand Macrocycle Induced by pH: A Computational Study.
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- International Journal of Molecular Sciences, 2016, v. 17, n. 7, p. 1131, doi. 10.3390/ijms17071131
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Catalytic Systems Based on the Metal Complexes of 1-Alkyl-4-Aza-1-Azoniabicyclo[2.2.2]Octane Bromides.
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- Kinetics & Catalysis, 2020, v. 61, n. 2, p. 269, doi. 10.1134/S0023158420010140
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Synthesis of 4′-alkyl-8-azaspiro[bicyclo[3.2.1]octane-3,2′-morpholin]-5′-ones.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 1, p. 87, doi. 10.1134/S1070428016010164
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Acylation of 1 H-1,2-diazaphenalenes with aliphatic carboxylic acid anhydrides.
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- Russian Journal of Organic Chemistry, 2016, v. 52, n. 1, p. 131, doi. 10.1134/S1070428016010255
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Syntheses, optical properties, and bioimaging application of near-infrared aza-BODIPY dyes with electronic push–pull system.
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- Research on Chemical Intermediates, 2023, v. 49, n. 7, p. 2955, doi. 10.1007/s11164-023-05028-0
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SBA-15-SOH-assisted preparation of 4-aza-phenanthrene-3,10-dione derivatives via a one-pot, four-component reaction.
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- Research on Chemical Intermediates, 2018, v. 44, n. 1, p. 739, doi. 10.1007/s11164-017-3131-0
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3-Chlorophenylboronic acid-promoted, one-pot, aza-Friedel-Crafts reaction of indoles.
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- Research on Chemical Intermediates, 2015, v. 41, n. 4, p. 2583, doi. 10.1007/s11164-013-1370-2
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Synthesis and anticancer activity of some new pyridine derivatives.
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- Research on Chemical Intermediates, 2012, v. 38, n. 7, p. 1291, doi. 10.1007/s11164-011-0413-9
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Unlocking New Prenylation Modes: Azaindoles as a New Substrate Class for Indole Prenyltransferases.
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- ChemCatChem, 2023, v. 15, n. 19, p. 1, doi. 10.1002/cctc.202300650
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Aza-Michael Reactions of Isatin Imines: Deeper Insight and Origin of the Stereoselectivity.
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- ChemCatChem, 2016, v. 8, n. 18, p. 2961, doi. 10.1002/cctc.201600584
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Searching for a new family of insensitive high explosives by introducing N hybridization and N-oxides into a cage cubane.
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- Journal of Molecular Modeling, 2014, v. 20, n. 11, p. 1, doi. 10.1007/s00894-014-2483-2
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A comparative study of the aromaticity of pyrrole, furan, thiophene, and their aza-derivatives.
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- Journal of Molecular Modeling, 2013, v. 19, n. 9, p. 3529, doi. 10.1007/s00894-013-1877-x
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Ethyl 2-(12-Oxo-10,12-dihydroisoindolo[1,2-b] Quinazolin-10-yl) Acetate.
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- Molbank, 2023, v. 2023, n. 2, p. M1628, doi. 10.3390/M1628
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4-Hydroxy-1-methyl-7-(propan-2-yl)-4-azatricyclo [5.2.2.02,6]undec-8-ene-3,5-dione.
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- Molbank, 2012, v. 12, n. 3, p. 1, doi. 10.3390/M767
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Insecticidal Evaluation and [4+2] Aza-Diels-Alder Synthesis of 3,7-Diaryl-6,7-dihydro-5 H-6-substituted Thiazolo[3,2-a]pyrimidin-5-ones Under Coupled Ultrasonic Irradiation and PTC.
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- Journal of Heterocyclic Chemistry, 2016, v. 53, n. 1, p. 38, doi. 10.1002/jhet.776
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Rapid, Eco-friendly, and.
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- Journal of Heterocyclic Chemistry, 2016, v. 53, n. 1, p. 164, doi. 10.1002/jhet.1811
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DBU Promoted Facile Synthesis of New Thieno[2,3- b]pyridine/quinoline Derivatives and Their Antimicrobial Evaluation.
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- Journal of Heterocyclic Chemistry, 2013, v. 50, p. E131, doi. 10.1002/jhet.1091
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Enantioselective Aza Michael-Type Addition to Alkenyl Benzimidazoles Catalyzed by a Chiral Phosphoric Acid.
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- Angewandte Chemie, 2016, v. 128, n. 3, p. 939, doi. 10.1002/ange.201508231
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Highly Enantioselective Aza-Michael Reaction between Alkyl Amines and β-Trifluoromethyl β-Aryl Nitroolefins.
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- Angewandte Chemie, 2015, v. 127, n. 51, p. 15634, doi. 10.1002/ange.201508371
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