A series of phosphine donor-stabilized N-silylphosphoranimine salts [R'3P.PR2=NSiMe3]+Br- were prepared from the direct reaction between the phosphoranimines BrR2P=NSiMe3 (R = Me, OCH2CF3) and the tertiary phosphines nBu3P and Me3P. The 1JPP values of these salts exhibit an unusual dependence on the substituents at the phosphoranimine acceptor and appear to reflect an electronic push-pull mecha...

The direct UV irradiation of cyclic phosphites 1–4 was carried out in argon-saturated solvents. In all cases examined, the rearranged, ring-contracted Photo-Arbuzov phosphonate was the major product formed with isolated yields ranging from 40 to 50%. These phosphonate photoproducts, 5–8, represent novel, bicyclic, aromatic phosphonate systems never before described in the literature of heterocy...

Abstract High enantioselectivities (up to 99 %) and activities (TOF's up >4000 h −1 ) are accomplished in the Pd‐catalyzed allylic substitution of a wide range substrate types nucleophiles using family phosphite‐oxazoline ligands. These ligands were derived from PHOX ligand by exchanging phosphine moieties biaryl phosphites methylene spacer was introduced between oxazoline phenyl ring. The s...

A homoleptic scandium trialkyl complex in combination with a borate compound served as an excellent catalyst for the C–H addition of aliphatic tertiary amines to olefins. This highly regiospecific, 100% atom efficient C–H bond alkylation reaction was applicable to a wide variety of tertiary amines and olefins, including functionalised styrenes and unactivated a-olefins. This work represents the...

A series of aluminum alkyl complexes nacnacRAlMe2 (2a-2h) bearing aliphatic N-substituted β-diketiminate ligands (nacnacRH = N,N'-dialkyl-2-amino-4-iminopent-2-enes), were prepared from the reaction of trialkyl aluminum and the corresponding β-diketimines. All these aluminum complexes were characterized by NMR, elemental analysis and HRMS spectroscopy. The molecular structures of complexes 2a, ...

A homoleptic scandium trialkyl complex in combination with a borate compound served as an excellent catalyst for the C-H addition of aliphatic tertiary amines to olefins. This highly regiospecific, 100% atom efficient C-H bond alkylation reaction was applicable to a wide variety of tertiary amines and olefins, including functionalised styrenes and unactivated α-olefins. This work represents the...

A stereoselective radical-mediated hydrogermylation of the protected 5-ethynyluracil nucleosides with trialkyl-, triaryl,- or tris(trimethylsilyl)germanes gave (Z)-5-(2-germylvinyl)uridine, 2'-deoxyuridine, or ara-uridine as major products. Reaction of the β-triphenylgermyl vinyl radical intermediate with oxygen and fragmentation of the resulting peroxyradical provided also 5-[2-(triphenylgermy...

The toxicities of a series of glycerol mono-, di-, and trialkyl ethers against Vibrio fischeri bacteria have been determined. A systematic study has been carried out and the possible structure–toxicity relationships have been discussed using different QSAR models. Inhibition of bioluminescence after 30 minutes of exposure shows relatively low toxicity of many of the glycerol derived chemicals s...

Mn(OAc)3-mediated tandem phosphonyl radical addition to β-nitrostyrenes followed by denitration to form (E)-2-alkenyl phosphonates in good yield is described.