“
“The diamagnetic cobalt(III) dimethyl complex, cis,mer-(PMe(3))(3)Co(CH(3))(2)I, click here was found to promote selective C-C bond formation, affording ethane and triplet (PMe(3))(3)CoI. The mechanism of reductive elimination has been investigated by a series of kinetic and isotopic-labeling experiments. Ethane formation proceeds with a rate constant of 3.1(5) x 10(-5) s(-1) (50 degrees C) and activation parameters of Delta H(double dagger) = 31.4(8) kcal/mol and Delta S(double dagger) = 17(3) eu. Addition of free trimethylphosphine or coordinating solvent

strongly inhibits reductive elimination, indicating reversible phosphine dissociation prior to C-C bond-coupling. EXSY NMR analysis established a rate constant of 9(2) s(-1) for phosphine loss from cis,mer-(PMe(3))(3)Co(CH(3))(2)I. Radical trapping, crossover, and isotope effect experiments were consistent with a proposed mechanism for ethane extrusion where formation of an unobserved five-coordinate intermediate is followed by concerted C-C bond formation. An unusual intermolecular exchange of cobalt-methyl ligands was also observed by isotopic labeling.”
“Background: Adjuvant hormone therapy (AHT) following radiotherapy or surgery is a treatment option frequently offered to men with localised or locally advanced prostate cancer. We performed a systematic review of published randomised trials

selleck kinase inhibitor to assess the effectiveness of AHT.\n\nMethods: We searched MEDLINE, EMBASE, the Cochrane library, SCI, LILACS and SIGLE for randomised trials comparing AHT plus primary therapy (radiotherapy or prostatectomy) with primary therapy alone. Data on study design, participants interventions and Outcomes were extracted from relevant studies and where possible pooled for meta-analysis.\n\nFindings: AHT following radiotherapy improved overall survival (at 5 years OR fixed effect model

1.29, 95% CI 1.07-1.56, p = 0.007), disease-specific survival (OR 2.10, 95% CI 1.53-2.88, p < 0.00001) and disease-free survival (OR 1.91, 95% CI 1.16-2.23, p < 0.00001). A random effect model favoured adjuvant hormone therapy but did not reach significance. After prostatectomy, there was no significant overall survival advantage with AHT, although one study reported a significant improvement in disease-specific survival (HR 4.09, p = 0.0004). Disease-free survival was also better with AHT (OR 3.73, 95% CI 2.30-6.03, p < 0.00001). AHT-induced Repotrectinib solubility dmso toxicities included gynaecomastia, impotence, gastrointestinal and haematological.\n\nConclusions: There are significant clinical benefits associated with the use of AHT for early prostate cancer. Patients should make an informed decision to accept AHT based on its effectiveness and side-effects. (C) 2009 Elsevier Ltd. All rights reserved.”
“Multiparous Stat1(-/-) mice spontaneously develop mammary tumors with increased incidence: at an average age of 12 months, 55% of the animals suffer from mammary cancer, although the histopathology is heterogeneous.