The Interlocking of Salicylic Aldehydes and Ketones with a 2 h ‐1,2,4,3‐Triazaphosphole
Author:
Affiliation:
1. Institut für Anorganische Chemie der Universität München, Meiserstraße 1, D‐80333 München, Germany
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19961291215
Reference16 articles.
1. 1,2,4,3-Triazaphosphole
2. 1,2,4,3λ3-Triazaphosphole durch reduktive (σ4 → σ2)-Eliminierung am Phosphor
3. 1,2,4,3λ3-Triazaphospholes Synthesized by Reductive(σ4→σ2)-Elimination at Phosphorus
4. In a preliminary account a spirocyclic structure was assumed for the product erroneously[3]. It could have resulted from a nucleophilic attack of the tervalent phosphorus atom in A onto the carbon atom of the carbonyl group and a subsequent proton shift from N to O stabilizing the zwitterion.
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1. Synthesis and Chemistry of 1,2,4,3-Triazaphosphole Derivatives;Current Organic Chemistry;2023-04
2. Syntheses of 1,2‐Oxaphospholane 2‐Oxides and 1,2‐Oxaphosphole 2‐Oxides;ChemistrySelect;2023-03-26
3. Bicyclic Systems with Bridgehead (Ring Junction) Phosphorus, Arsenic, Antimony, or Bismuth Atoms;Comprehensive Heterocyclic Chemistry III;2008
4. Three or Four Heteroatoms including at least One Phosphorus;Comprehensive Heterocyclic Chemistry III;2008
5. N-Heterosubstituted Iminoacyl Functions;Comprehensive Organic Functional Group Transformations II;2005
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