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sprühen Gespenstisch Dämon azetidine ring opening Würstchen Randalieren brechen

Catalytic enantioselective intermolecular desymmetrization of azetidines. |  Semantic Scholar
Catalytic enantioselective intermolecular desymmetrization of azetidines. | Semantic Scholar

Azetidine - an overview | ScienceDirect Topics
Azetidine - an overview | ScienceDirect Topics

Molecules | Free Full-Text | Synthesis of 2-Oxazolines from Ring Opening  Isomerization of 3-Amido-2-Phenyl Azetidines
Molecules | Free Full-Text | Synthesis of 2-Oxazolines from Ring Opening Isomerization of 3-Amido-2-Phenyl Azetidines

Acid-Mediated Ring Expansion of 2,2-Disubstituted Azetidine Carbamates to  6,6-Disubstituted 1,3-Oxazinan-2-ones | Organic Letters
Acid-Mediated Ring Expansion of 2,2-Disubstituted Azetidine Carbamates to 6,6-Disubstituted 1,3-Oxazinan-2-ones | Organic Letters

Intramolecular Ring-Opening Decomposition of Aryl Azetidines | ACS  Medicinal Chemistry Letters
Intramolecular Ring-Opening Decomposition of Aryl Azetidines | ACS Medicinal Chemistry Letters

Azetidine-2-Carboxylic Acid - an overview | ScienceDirect Topics
Azetidine-2-Carboxylic Acid - an overview | ScienceDirect Topics

Anionic Ring-Opening Polymerization of N-(tolylsulfonyl)azetidines To  Produce Linear Poly(trimethylenimine) and Closed-System Block Copolymers |  Journal of the American Chemical Society
Anionic Ring-Opening Polymerization of N-(tolylsulfonyl)azetidines To Produce Linear Poly(trimethylenimine) and Closed-System Block Copolymers | Journal of the American Chemical Society

Regioselective ring opening reactions of azetidines | Download Scientific  Diagram
Regioselective ring opening reactions of azetidines | Download Scientific Diagram

The anionic ring-opening polymerization of N-(methanesulfonyl)azetidine -  Polymer Chemistry (RSC Publishing)
The anionic ring-opening polymerization of N-(methanesulfonyl)azetidine - Polymer Chemistry (RSC Publishing)

Recent advances in synthetic facets of immensely reactive azetidines
Recent advances in synthetic facets of immensely reactive azetidines

Chiral donor–acceptor azetines as powerful reactants for synthesis of amino  acid derivatives | Nature Communications
Chiral donor–acceptor azetines as powerful reactants for synthesis of amino acid derivatives | Nature Communications

Metabolism of Strained Rings: Glutathione S-transferase–Catalyzed Formation  of a Glutathione-Conjugated Spiro-azetidine without Prior Bioactivation |  Drug Metabolism & Disposition
Metabolism of Strained Rings: Glutathione S-transferase–Catalyzed Formation of a Glutathione-Conjugated Spiro-azetidine without Prior Bioactivation | Drug Metabolism & Disposition

Azetidines of pharmacological interest - Parmar - 2021 - Archiv der  Pharmazie - Wiley Online Library
Azetidines of pharmacological interest - Parmar - 2021 - Archiv der Pharmazie - Wiley Online Library

Aziridines and azetidines: building blocks for polyamines by anionic and  cationic ring-opening polymerization - ScienceDirect
Aziridines and azetidines: building blocks for polyamines by anionic and cationic ring-opening polymerization - ScienceDirect

Ring‐Opening of Carbamate‐Protected Aziridines and Azetidines in Liquid  Sulfur Dioxide - Lugiņina - 2016 - European Journal of Organic Chemistry -  Wiley Online Library
Ring‐Opening of Carbamate‐Protected Aziridines and Azetidines in Liquid Sulfur Dioxide - Lugiņina - 2016 - European Journal of Organic Chemistry - Wiley Online Library

Molbank | Free Full-Text | Photoinduced Ring Opening of Methyl  1-Aryl-5-oxo-6,7-dihydro-1H,5H-pyrazolo[1,2-a]pyrazole-2-carboxylates in  the Presence of Diaryl Disulfides
Molbank | Free Full-Text | Photoinduced Ring Opening of Methyl 1-Aryl-5-oxo-6,7-dihydro-1H,5H-pyrazolo[1,2-a]pyrazole-2-carboxylates in the Presence of Diaryl Disulfides

Aziridines and azetidines: building blocks for polyamines by anionic and  cationic ring-opening polymerization
Aziridines and azetidines: building blocks for polyamines by anionic and cationic ring-opening polymerization

Regio- and Stereoselective Ring Opening of Enantiomerically Enriched 2-Aryl  Oxetanes and 2-Aryl Azetidines with Aryl Borates | The Journal of Organic  Chemistry
Regio- and Stereoselective Ring Opening of Enantiomerically Enriched 2-Aryl Oxetanes and 2-Aryl Azetidines with Aryl Borates | The Journal of Organic Chemistry

Azetidine-2-Carboxylic Acid - an overview | ScienceDirect Topics
Azetidine-2-Carboxylic Acid - an overview | ScienceDirect Topics

Synthesis of azetidines by aza Paternò–Büchi reactions - Chemical Science  (RSC Publishing) DOI:10.1039/D0SC01017K
Synthesis of azetidines by aza Paternò–Büchi reactions - Chemical Science (RSC Publishing) DOI:10.1039/D0SC01017K

The anionic ring-opening polymerization of N -(methanesulfonyl)azetidine -  Polymer Chemistry (RSC Publishing) DOI:10.1039/C8PY00074C
The anionic ring-opening polymerization of N -(methanesulfonyl)azetidine - Polymer Chemistry (RSC Publishing) DOI:10.1039/C8PY00074C

Azetidiniums: Ring‐Expansion to Pyrrolidines, Piperidines, Azepanes, and  Azocanes - Masson - 2020 - European Journal of Organic Chemistry - Wiley  Online Library
Azetidiniums: Ring‐Expansion to Pyrrolidines, Piperidines, Azepanes, and Azocanes - Masson - 2020 - European Journal of Organic Chemistry - Wiley Online Library

Synthesis of optically active 2-substituted azetidine-2-carbonitriles from  chiral 1-arylethylamine via α-alkylation of N -borane complexes - RSC  Advances (RSC Publishing) DOI:10.1039/D1RA04585G
Synthesis of optically active 2-substituted azetidine-2-carbonitriles from chiral 1-arylethylamine via α-alkylation of N -borane complexes - RSC Advances (RSC Publishing) DOI:10.1039/D1RA04585G