Publications by authors named "K OKANO"

Objective: Limitations are sometimes encountered in the application of laparoscopic cholecystectomy to the treatment of acute cholecystitis. Endoscopic gallbladder stenting (EGBS) has emerged as an additional option. However, the long-term stent patency remains an issue.

View Article and Find Full Text PDF

Background: The implementation of cancer precision medicine in Japan is deeply intertwined with insurance reimbursement policies and requires case-by-case reviews by Molecular Tumor Boards (MTBs), which impose considerable operational burdens on healthcare facilities. The extensive preparation and review times required by MTBs hinder their ability to efficiently assess comprehensive genomic profiling (CGP) test results. Despite attempts to optimize MTB operations, significant challenges remain.

View Article and Find Full Text PDF

The C-H arylation of 2-quinolinecarboxyamide bearing a C-Br bond at the -aryl moiety is carried out with a palladium catalyst. The reaction proceeds at the C-H bond on the pyridine ring adjacent to the amide group in the presence of 10 mol % Pd(OAc) at 110 °C to afford the cyclized product in 42% yield. The yield is improved to 94% when the reaction is performed with PPh as a ligand of palladium.

View Article and Find Full Text PDF
Article Synopsis
  • The study compares the effectiveness of sequencing-batch reactors (SBRs) and continuous-flow reactors (CFRs) in removing dissolved manganese (Mn) from mine drainage using manganese-oxidizing bacteria.
  • SBRs showed superior performance, achieving over 66% Mn removal in four weeks, while CFRs reached only about 13.6%, highlighting higher microbial activity in SBRs during the start-up phase.
  • Both reactors produced mixed manganese-oxide deposits, but SBRs had a slightly higher average oxidation valence, with different microbial communities dominating the early stages and steady state, indicating distinct pathways for manganese oxidation.
View Article and Find Full Text PDF

A three-component synthesis of multiply functionalized 5,6-dehydroisoquinuclidines is described. After the formation of an -alkylpyridinium salt, Grignard addition led to the formation of the corresponding 1,2-dihydropyridine bearing an alkyl, alkene, aryl, or alkynyl group. Subsequent Diels-Alder reaction with a dienophile provided functionalized dehydroisoquinuclidines in high yields (up to 93%) with selectivities (73:27 to >99:1).

View Article and Find Full Text PDF