1-PHOSPHA-2-AZANORBORNENE AS PRECURSOR FOR 1-PHOSPHA-BICYCLO[3.2.1]OCTA-2,5-DIENE

Authors

  • Peter WONNEBERGER Institute of Inorganic Chemistry, Faculty of Chemistry, Leipzig University, Johannisallee 29, 04103 Leipzig, Germany. https://orcid.org/0009-0003-5084-4041
  • Lydia KEIL Institute of Inorganic Chemistry, Faculty of Chemistry, Leipzig University, Johannisallee 29, 04103 Leipzig, Germany.
  • Paul SPICKENREUTHER Institute of Inorganic Chemistry, Faculty of Chemistry, Leipzig University, Johannisallee 29, 04103 Leipzig, Germany.
  • Peter LÖNNECKE nstitute of Inorganic Chemistry, Faculty of Chemistry, Leipzig University, Johannisallee 29, 04103 Leipzig, Germany https://orcid.org/0009-0003-5084-4041
  • Evamarie HEY-HAWKINS Faculty of Chemistry and Chemical Engineering, Babeş-Bolyai University, 11 Arany Janos str., RO-400028, Cluj-Napoca, Romania; Institute of Bioanalytical Chemistry, Faculty of Chemistry, Leipzig University, Deutscher Platz 5, 04103 Leipzig, Germany, *evamarie.hey@ubbcluj.ro https://orcid.org/0009-0003-5084-4041

DOI:

https://doi.org/10.24193/subbchem.2025.4.17

Keywords:

P-heterocycles, phosphanes, reduction, ring expansion, sulfonamides

Abstract

1-Phospha-2-azanorbornenes, the cycloaddition products of 2H-phospholes with a sulfonyl imine, can be converted to 1-phospha-bicyclo[3.2.1]octa-2,5-dienes by a reductive rearrangement. This reaction is, however, dependent on the substituent R in a-position. While a clean reaction is observed for R = H or Ph, the 2-pyridyl derivative leads to a complex product mixtures.

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Published

2025-12-16

How to Cite

WONNEBERGER, P., KEIL, L., SPICKENREUTHER, P., LÖNNECKE, P., & HEY-HAWKINS, E. (2025). 1-PHOSPHA-2-AZANORBORNENE AS PRECURSOR FOR 1-PHOSPHA-BICYCLO[3.2.1]OCTA-2,5-DIENE. Studia Universitatis Babeș-Bolyai Chemia, 70(4), 293–299. https://doi.org/10.24193/subbchem.2025.4.17

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