(Figure Presented) Strong yet gentle: Where triflate reagents fail, carborane-based sources of H+, CH3+, and [R3Si]+ electrophiles add to phosphabenzenes preferentially at the P atom rather than C (see picture). © 2008 Wiley-VCH Verlag GmbH & Co. KGaA
© 2016 Taylor & Francis Group, LLC.The Michael-type addition of tertiary phosphines to electron-defi...
Weber L, Dembeck G, Stammler H-G, Neumann B, Schmidtmann M, Müller A. Protonation and Alkylation Rea...
This thesis outlines the results from the projects undertaken as a part of my PhD studies: the synth...
(Figure Presented) Strong yet gentle: Where triflate reagents fail, carborane-based sources of H+, C...
For decades, triflic acid, methyl triflate, and trialkylsilyl triflate reagents have served syntheti...
Weitkamp R, Neumann B, Stammler H-G, Hoge B. Phosphorus-containing Superbases: Recent Progress in th...
Si(mply) rips it apart: C-F activation of fluorobenzene has been achieved using the extremely strong...
Weber L, Meyer M, Quasdorff B. Reactivity of phosphaalkenes toward carbene complexes. Phosphorus, Su...
NIECKE E, RUGER R, Schoeller W. PHOSPHAZENES WITH COORDINATION NUMBERS 2 AND 3 .23. "TERT-BUTYLIMINO...
Cations derived from (NPCl2)3, hexachloro-cyclo-triphosphazene, the weakly basic precursor of phosph...
The simplest parent phosphinidene, :PH (<b>1</b>), has been observed only in the gas phase or low te...
Our work reflects efforts to increase the Lewis acidity of two-coordinate phosphorus(III)-based comp...
Trimethylsilyl-substituted triazaphospholes were synthesized by a [3+2] cycloaddition reaction betwe...
Phosphorus compounds have a rich chemical history as Lewis donor ligands in transition metal and org...
Vignolle J, Gornitzka H, Maron L, Schoeller W, Bourissou D, Bertrand G. Transient palladadiphosphany...
© 2016 Taylor & Francis Group, LLC.The Michael-type addition of tertiary phosphines to electron-defi...
Weber L, Dembeck G, Stammler H-G, Neumann B, Schmidtmann M, Müller A. Protonation and Alkylation Rea...
This thesis outlines the results from the projects undertaken as a part of my PhD studies: the synth...
(Figure Presented) Strong yet gentle: Where triflate reagents fail, carborane-based sources of H+, C...
For decades, triflic acid, methyl triflate, and trialkylsilyl triflate reagents have served syntheti...
Weitkamp R, Neumann B, Stammler H-G, Hoge B. Phosphorus-containing Superbases: Recent Progress in th...
Si(mply) rips it apart: C-F activation of fluorobenzene has been achieved using the extremely strong...
Weber L, Meyer M, Quasdorff B. Reactivity of phosphaalkenes toward carbene complexes. Phosphorus, Su...
NIECKE E, RUGER R, Schoeller W. PHOSPHAZENES WITH COORDINATION NUMBERS 2 AND 3 .23. "TERT-BUTYLIMINO...
Cations derived from (NPCl2)3, hexachloro-cyclo-triphosphazene, the weakly basic precursor of phosph...
The simplest parent phosphinidene, :PH (<b>1</b>), has been observed only in the gas phase or low te...
Our work reflects efforts to increase the Lewis acidity of two-coordinate phosphorus(III)-based comp...
Trimethylsilyl-substituted triazaphospholes were synthesized by a [3+2] cycloaddition reaction betwe...
Phosphorus compounds have a rich chemical history as Lewis donor ligands in transition metal and org...
Vignolle J, Gornitzka H, Maron L, Schoeller W, Bourissou D, Bertrand G. Transient palladadiphosphany...
© 2016 Taylor & Francis Group, LLC.The Michael-type addition of tertiary phosphines to electron-defi...
Weber L, Dembeck G, Stammler H-G, Neumann B, Schmidtmann M, Müller A. Protonation and Alkylation Rea...
This thesis outlines the results from the projects undertaken as a part of my PhD studies: the synth...
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