Abstract A novel and convenient procedure for the oxidative cyclization of diols to the corresponding lactones was achieved using trichloro- and tribromoisocyanuric acids. The methodology provided 5–11-membered lactones in 50–98% yield under simple and mild conditions. A reaction pathway is proposed by experimental evidence and DFT calculations at M062x/6-311G(d,p) level. Graphical abstract
Building similarity graph...
Analyzing shared references across papers
Loading...
Carlos Vinícius P. dos Santos
Raphael C. Alves
Marcio C. S. de Mattos
Monatshefte für Chemie - Chemical Monthly
Universidade Federal do Rio de Janeiro
Universidade Federal Rural do Rio de Janeiro
Building similarity graph...
Analyzing shared references across papers
Loading...
Santos et al. (Tue,) studied this question.
synapsesocial.com/papers/69a75a6dc6e9836116a20362 — DOI: https://doi.org/10.1007/s00706-026-03432-x
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: