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Leistung montieren im Uhrzeigersinn aziridine ring opening Hetzen Veteran Gefängnis

Highly regioselective ring-opening of aziridines with arenesulfinates on  water: a facile access to β-amino/vinyl sulfones - ScienceDirect
Highly regioselective ring-opening of aziridines with arenesulfinates on water: a facile access to β-amino/vinyl sulfones - ScienceDirect

N-methylative aziridine ring opening and the synthesis of  (S)-3-methylamino-3-[(R)-pyrrolidin-3-yl]propanenitrile - ScienceDirect
N-methylative aziridine ring opening and the synthesis of (S)-3-methylamino-3-[(R)-pyrrolidin-3-yl]propanenitrile - ScienceDirect

Aziridines and azetidines: building blocks for polyamines by anionic and  cationic ring-opening polymerization - Polymer Chemistry (RSC Publishing)  DOI:10.1039/C9PY00278B
Aziridines and azetidines: building blocks for polyamines by anionic and cationic ring-opening polymerization - Polymer Chemistry (RSC Publishing) DOI:10.1039/C9PY00278B

Regioselective Synthesis of N-β-Hydroxyethylaziridines by the Ring-Opening  Reaction of Epoxides with Aziridine Generated in Situ
Regioselective Synthesis of N-β-Hydroxyethylaziridines by the Ring-Opening Reaction of Epoxides with Aziridine Generated in Situ

Nucleophilic ring opening reactions of aziridines | SpringerLink
Nucleophilic ring opening reactions of aziridines | SpringerLink

Molecules | Free Full-Text | Aziridine Ring Opening as Regio- and  Stereoselective Access to C-Glycosyl-Aminoethyl Sulfide Derivatives
Molecules | Free Full-Text | Aziridine Ring Opening as Regio- and Stereoselective Access to C-Glycosyl-Aminoethyl Sulfide Derivatives

Iron-Catalyzed Ring-Opening of meso-Aziridines with Amines
Iron-Catalyzed Ring-Opening of meso-Aziridines with Amines

Catalyst‐Free Regio‐ and Stereospecific Synthesis of β‐Sulfonamido  Dithiocarbamates: Efficient Ring‐Opening Reactions of N‐Tosyl Aziridines by  Dialkyldithiocarbamates - Alagiri - 2011 - Chemistry – A European Journal -  Wiley Online Library
Catalyst‐Free Regio‐ and Stereospecific Synthesis of β‐Sulfonamido Dithiocarbamates: Efficient Ring‐Opening Reactions of N‐Tosyl Aziridines by Dialkyldithiocarbamates - Alagiri - 2011 - Chemistry – A European Journal - Wiley Online Library

Modular, One-Pot, Sequential Aziridine Ring Opening-S(N)Ar Strategy to 7-,  10-, and 11-Membered Benzo-Fused Sultams. - Abstract - Europe PMC
Modular, One-Pot, Sequential Aziridine Ring Opening-S(N)Ar Strategy to 7-, 10-, and 11-Membered Benzo-Fused Sultams. - Abstract - Europe PMC

PDF] Recent applications of aziridine ring expansion reactions in  heterocyclic synthesis | Semantic Scholar
PDF] Recent applications of aziridine ring expansion reactions in heterocyclic synthesis | Semantic Scholar

Regioselective Ring‐Opening Nucleophilic Addition of Aziridines through  Photoredox Catalyst - Sun - 2014 - Advanced Synthesis & Catalysis -  Wiley Online Library
Regioselective Ring‐Opening Nucleophilic Addition of Aziridines through Photoredox Catalyst - Sun - 2014 - Advanced Synthesis & Catalysis - Wiley Online Library

PDF] Recent applications of aziridine ring expansion reactions in  heterocyclic synthesis | Semantic Scholar
PDF] Recent applications of aziridine ring expansion reactions in heterocyclic synthesis | Semantic Scholar

Enantioselective fluoride ring opening of aziridines enabled by cooperative  Lewis acid catalysis - ScienceDirect
Enantioselective fluoride ring opening of aziridines enabled by cooperative Lewis acid catalysis - ScienceDirect

Regioselective ring opening of aziridine-fused... | Download Scientific  Diagram
Regioselective ring opening of aziridine-fused... | Download Scientific Diagram

Molecules | Free Full-Text | Alkylative Aziridine Ring-Opening Reactions
Molecules | Free Full-Text | Alkylative Aziridine Ring-Opening Reactions

Scheme 3. Regioselective ring-opening reactions of the [3.1.0] bicyclic...  | Download Scientific Diagram
Scheme 3. Regioselective ring-opening reactions of the [3.1.0] bicyclic... | Download Scientific Diagram

Aziridines - Wikipedia
Aziridines - Wikipedia

Aziridines - Wikipedia
Aziridines - Wikipedia

Intermolecular [3+3] ring expansion of aziridines to dehydropiperi-dines  through the intermediacy of aziridinium ylides | Nature Communications
Intermolecular [3+3] ring expansion of aziridines to dehydropiperi-dines through the intermediacy of aziridinium ylides | Nature Communications

Unprecedented carbon–carbon bond cleavage in nucleophilic aziridine ring  opening reaction, efficient ring transformation of aziridines to  imidazolidin-4-ones - Chemical Communications (RSC Publishing)
Unprecedented carbon–carbon bond cleavage in nucleophilic aziridine ring opening reaction, efficient ring transformation of aziridines to imidazolidin-4-ones - Chemical Communications (RSC Publishing)

Highly efficient regio-selective ring-opening nucleophilic fluorination of  aziridines and azetidines: access to β- or γ-fluorinated amino acid  derivatives - Organic & Biomolecular Chemistry (RSC Publishing)
Highly efficient regio-selective ring-opening nucleophilic fluorination of aziridines and azetidines: access to β- or γ-fluorinated amino acid derivatives - Organic & Biomolecular Chemistry (RSC Publishing)

Molecules | Free Full-Text | Alkylative Aziridine Ring-Opening Reactions |  HTML
Molecules | Free Full-Text | Alkylative Aziridine Ring-Opening Reactions | HTML

Nucleophilic ring opening reactions of aziridines | Semantic Scholar
Nucleophilic ring opening reactions of aziridines | Semantic Scholar

File:Aziridine ring opening.svg - Wikipedia
File:Aziridine ring opening.svg - Wikipedia

Regiochemistry in aziridine ring opening reactions. | Download Scientific  Diagram
Regiochemistry in aziridine ring opening reactions. | Download Scientific Diagram

Nucleophilic ring opening of aziridines with amines under catalyst- and  solvent-free conditions - Green Chemistry (RSC Publishing)
Nucleophilic ring opening of aziridines with amines under catalyst- and solvent-free conditions - Green Chemistry (RSC Publishing)

File:Aziridine opening.png - Wikimedia Commons
File:Aziridine opening.png - Wikimedia Commons