1994
DOI: 10.1002/chin.199411222
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ChemInform Abstract: 1,8‐Diazabicyclo(5.4.0)undecene‐Mediated Transesterification of p‐ Nitrophenyl Phosphonates: A Novel Route to Phosphono Esters.

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“…The synthesis of fluorophosphonate 3 is depicted in Figure 2 and commences with the standard three-step conversion of 11bromoundecanol (4) into N-Boc-11-aminoundecan-1-ol (5). Treatment of the latter compound with di-p-nitrophenyl methylphosphonate and DBU gave methylphosphonate 6 in good overall yield (21). At this stage, the O-p-nitrophenyl group in (6) was substituted for fluorine using tetrabutylammonium triphenyldifluorosilicate (TBAT) as the dry fluorine source, giving fluorophosphonate 7 in 70% yield.…”
Section: Resultsmentioning
confidence: 99%
“…The synthesis of fluorophosphonate 3 is depicted in Figure 2 and commences with the standard three-step conversion of 11bromoundecanol (4) into N-Boc-11-aminoundecan-1-ol (5). Treatment of the latter compound with di-p-nitrophenyl methylphosphonate and DBU gave methylphosphonate 6 in good overall yield (21). At this stage, the O-p-nitrophenyl group in (6) was substituted for fluorine using tetrabutylammonium triphenyldifluorosilicate (TBAT) as the dry fluorine source, giving fluorophosphonate 7 in 70% yield.…”
Section: Resultsmentioning
confidence: 99%