“…This produced the corresponding BODIPY- O -methyl oximes 9a–c in good yields (81%, 84%, and 74%, respectively). 43 Compounds 9a and 9b were obtained as single stereoisomers while 9c exhibited a 6 : 1 mixture of isomers at the oxime double bond, as determined by 1 H-NMR spectroscopy.…”
The neoglycosylation of methoxyaminomethyl BODIPYs with unprotected reducing saccharides produces cyclic N-glycosyl-N-methoxy-BODIPY conjugates, which display excellent photophysical characteristics in pure water, even at high dye concentrations.
“…This produced the corresponding BODIPY- O -methyl oximes 9a–c in good yields (81%, 84%, and 74%, respectively). 43 Compounds 9a and 9b were obtained as single stereoisomers while 9c exhibited a 6 : 1 mixture of isomers at the oxime double bond, as determined by 1 H-NMR spectroscopy.…”
The neoglycosylation of methoxyaminomethyl BODIPYs with unprotected reducing saccharides produces cyclic N-glycosyl-N-methoxy-BODIPY conjugates, which display excellent photophysical characteristics in pure water, even at high dye concentrations.
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