Efficacy of immune checkpoint inhibitor combination therapy prior to nephrectomy in advanced renal cell carcinoma: A retrospective pilot study.

Renal cell carcinoma (RCC) affects 10%-20% of patients annually, often with metastases present. This study evaluated the impact of systemic therapy before nephrectomy in patients with unresectable or metastatic renal cell carcinoma (RCC). Patients receiving upfront immune checkpoint inhibitor (ICI) combination therapy showed significantly improved progression-free survival (PFS) compared to nephrectomy alone (2-year PFS: 62.

Ru(0)-catalysed synthesis of borylated polyene building blocks by cross-dimerisation toward cross-coupling.

Conjugated and non-conjugated polyenes are important substructures and are often found in biologically active compounds and natural products. Their preparation often needs multiple steps or iterative reactions and as a result, they have poor step economies. In this feature article, we show a new methodology to prepare these substructures by combinations of cross-dimerisation giving borylated polyenes and subsequent cross-coupling reactions.

Direct synthesis of conjugated tetraenes from 1,3-enynes with 1,3-dienes.

New direct access to conjugated tetraenes has been achieved. A Ru(0)-catalysed reaction of 1,3-enynes with 1,3-dienes gives 1,3,5,7-octatetraene derivatives by formal regioselective insertion of the alkynyl group of 1,3-enynes into the terminal C-H bond in 1,3-dienes. With a silyl substituent on the alkynyl side in 1,3-enynes, the reaction regioselectively proceeds to give the linear cross-dimerisation product having the silyl group at the internal position.

Halogen-, oxidant- and directing group-free synthesis of donor-acceptor type conjugated polymers.

An intermolecular hydrogen migration from dibutadienylpyridine to dialkynylthiophene catalysed by [Ru(-naphthalene)(-oxa-bnd)] (oxa-bnd = 9-oxabicyclo[3.3.1]nona-2,6-diene) produces poly(dialkynylthiophene--dibutadienylpyridine).

Ru(0)-catalysed cross-dimerisation and -trimerisation of alkynyl- with butadienylheteroarenes.

Ru(0)-catalysed cross-dimerisation and -trimerisation give a series of di- and triheteroaryl compounds cross-linked by π-conjugated trienyl groups. Their photochemical behaviour is studied using UV-visible absorption spectra, fluorescence emission spectra, and TD-DFT calculations. The cross-trimer prepared from 2,5-dialkynylthiophene with 2 equiv.