Chlorination of antibiotic fortimicin A with triphenylphosphine and carbon tetrachloride has been attempted, and 2-chloro-, 2,5-dichloro-, and 2-chloro-4-ene derivatives have been obtained. Successive dehalogenation of the chlorinated fortimicins A with tributylstannane gave the corresponding deoxyfortimicins A. Among five deoxyfortimicins A, 2-deoxyfortimicin A exhibits improved antimicrobial ...

Treatment of [PtI2(COD)] (COD = 1,5-cyclooctadiene) with 2-LiC6H4P(S)Ph2 gives the complex cis-[Pt{κ(2)-2-C6H4P(S)Ph2}2] () containing a pair of ortho-metallated triphenylphosphine sulfide rings. The selenium counterpart, [Pt{κ(2)-2-C6H4P(Se)Ph2}2] (), which exists as cis- and trans-isomers in solution, and the palladium analogues, cis-[Pd{κ(2)-2-C6H4P(X)Ph2}2] [X = S (), Se ()], are obtained b...

Refluxing a slightly acidic /?-BuOH solution of RhCKPPh,), and 2-chloro-, 2,4-dichloro-, or 2,4,6-trichloroazobenzene affords cyclometalated complexes (1) via loss of one phosphine ligand and oxidative addition of the ortho -C-Cl bond. X-ray structural analysis indicates a frcws-position of the two triphenylphosphine ligands. The reaction proceeds only in polar solvents like alcohols or dimethy...

Gold nanoparticles (AuNPs) can be evenly deposited on single-walled carbon nanotubes (SWCNTs) via the reduction of the highly stable complex, chloro(triphenylphosphine) gold(I), with SWCNT anions ('nanotubides'). This methodology highlights the unusual chemistry of nanotubides and provides a blueprint for the generation of many other hybrid nanomaterials.

Vicinal bis(trifluoroacetimidoyl chloride)s, a novel kind of fluorinated building block, were obtained from o-phenylenediamines in the presence of TFA, triethylamine, triphenylphosphine and tetrachloromethane. Based on these blocks, a new synthesis involving [2 + 2 + 2] cycloaddition reactions for trifluoromethylated benzo-fused eight-membered rings was disclosed.

Oxo-sulfido- and oxo-selenido-molybdenum(VI) complexes with an ene-1,2-dithiolate ligand are generated as models of the active sites of molybdenum hydroxylases. The sulfide and selenide groups are highly reactive toward triphenylphosphine in the order of Se > S.

Simple and rapid synthesis of various diversely functionalized unprotected 4-amino-2-chloroquinoline-3-aryl derivatives were synthesized in high yields by Suzuki cross-coupling reaction using microwave irradiation in water and in presence of tetrakis(triphenylphosphine)palladium(0). Electronic effects of o-substituted functional groups on the reaction were studied conclusively.

The thio-additions of glycals were efficiently promoted by a stoichiometric amount of trimethylsilyl bromide (TMSBr) to produce S-2-deoxyglycosides under solvent-free conditions in good to excellent yields. In addition, with triphenylphosphine oxide as an additive, the TMSBr-mediated direct glycosylations of glycals with a large range of alcohols were highly α-selective.

2-Acetylcyclopentanone undergoes a smooth reaction with triphenylphosphine and dialkyl acetylenedicarboxylates to produce dialkyl 2-(1-acetyl-2-oxocyclopentyl)-3-(1,1,1-triphenyl-lambda(5)-phosphanylidene)succinates. These compounds undergo intramolecular Wittig reactions in boiling benzene to produce highly strained spirocyclobutene derivatives, which spontaneously undergo ring-opening reactio...