The Interlocking of Salicylic Aldehydes and Ketones with a 2 h ‐1,2,4,3‐Triazaphosphole

Author:

Schmidpeter Alfred1,Steinmüller Franz1,Nöth Heinrich1

Affiliation:

1. Institut für Anorganische Chemie der Universität München, Meiserstraße 1, D‐80333 München, Germany

Publisher

Wiley

Subject

Inorganic Chemistry

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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