Azide-Free Synthesis of N‐Alkyliminophosphoranes from Phosphines and Hydroxylamine Derivatives
Open access
Date
2023-03-17Type
- Journal Article
Abstract
A broadly applicable and efficient method for the synthesis of N-alkyliminophosphoranes from phosphines that does not use potentially hazardous alkyl azides is reported. Under iron catalysis, a hydroxylamine-derived triflic acid salt oxidizes phosphines to a wide range of iminophosphorane triflic acid salts. Diphosphines afford phosphine-iminophosphoranes that can serve as ligands in transition metal complexes. The developed method can be employed in the synthesis of mixed diiminophosphoranes and in a traceless Staudinger ligation. Show more
Permanent link
https://doi.org/10.3929/ethz-b-000604760Publication status
publishedExternal links
Journal / series
Organic LettersVolume
Pages / Article No.
Publisher
American Chemical SocietyOrganisational unit
09634 - Morandi, Bill / Morandi, Bill
Funding
184658 - Catalytic synthesis of unprotected amines and heterocycles (SNF)
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