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Azetidines. 5. Reaction of 1,1,3,3-tetramethyl- and 1-benzyl-1,3,3-trimethylazetidinium ions with butyllithium and phenyllithium. Deuterium labeling as a mechanistic probe

https://doi.org/10.1021/jo01300a046
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inferred← citeshttps://doi.org/10.2139/ssrn.4048911openalex-extracted
inferred← citeshttps://doi.org/10.1002/9780470187197.ch1openalex-snapshot
Azetidines
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inferred← citeshttps://doi.org/10.1002/ange.202411555openalex-snapshot
A Strategy for the Formal C−N Cross‐Coupling of Tertiary Amines
inferred← citeshttps://doi.org/10.1002/anie.200904527openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.202411555openalex-snapshot
A Strategy for the Formal C−N Cross‐Coupling of Tertiary Amines
inferred← citeshttps://doi.org/10.1002/chem.201200167openalex-snapshot
Regioselective Cycloaddition of 3‐Azetidinones and 3‐Oxetanones with Alkynes through Nickel‐Catalysed Carbon–Carbon Bond Activation
inferred← citeshttps://doi.org/10.1002/chem.202301866openalex-snapshot
Impact of Catalyst Deuteration on the Reactivity of Chiral Phase‐Transfer Organocatalysts
inferred← citeshttps://doi.org/10.1002/chin.198044223openalex-snapshot
ChemInform Abstract: AZETIDINES. 5. REACTION OF 1,1,3,3‐TETRAMETHYL‐ AND 1‐BENZYL‐1,3,3‐TRIMETHYLAZETIDINIUM IONS WITH BUTYLLITHIUM AND PHENYLLITHIUM. DEUTERIUM LABELING AS A MECHANISTIC PROBE
inferred← citeshttps://doi.org/10.1002/ejoc.200600362openalex-snapshot
Ring Expansions of 2‐Alkenylazetidinium Salts – a New Route to Pyrrolidines and Azepanes
inferred← citeshttps://doi.org/10.1002/ejoc.201301536openalex-snapshot
Synthesis of 2‐Phenyl‐ and 2,2‐Diarylpyrrolidines through Stevens Rearrangement Performed on Azetidinium Ions
inferred← citeshttps://doi.org/10.1007/7081_2015_146openalex-snapshot
Ring Expansions of Nonactivated Aziridines and Azetidines
inferred← citeshttps://doi.org/10.1007/bf01431115openalex-snapshot
1,3-Dipolar cycloaddition ofin situ generated 2,2-dimethyl-and 2,2-dichlorodiazocyclopropanes to 3,3-dimethylcyclopropene
inferred← citeshttps://doi.org/10.1016/j.tet.2019.130661openalex-snapshot
Investigations of an annulation-fragmentation-spirocyclisation approach to fawcettimine-type Lycopodium alkaloids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.07.113openalex-snapshot
Synthesis and reactivity of enantiomerically pure N-alkyl-2-alkenyl azetidinium salts
inferred← citeshttps://doi.org/10.1016/j.tetlet.2006.11.175openalex-snapshot
Chemo- and regioselective reductive opening of azetidinium ions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2007.10.105openalex-snapshot
Opening of azetidinium ions with C-nucleophiles
inferred← citeshttps://doi.org/10.1016/j.tetlet.2022.153753openalex-snapshot
Synthesis of optically pure, deuterated Maruoka Catalysts and their chemical reactivity
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Lithium annual survey covering the year 1980
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Synthesis of 2,2-dialkylcyclopropylamines from β-chloroimines and application towards the synthesis of1-amino-2,2-dialkylcyclopropane-carboxylic acids
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Dienophilicity of Imidazole in Inverse Electron Demand Diels−Alder Reactions. 4. Intermolecular Reactions with 1,2,4-Triazines
inferred← citeshttps://doi.org/10.1021/jo9001323openalex-snapshot
One-Carbon Ring Expansion of Azetidines via Ammonium Ylide [1,2]-Shifts: A Simple Route to Substituted Pyrrolidines
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