2014
DOI: 10.2174/1570179411999140304142747
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The Addition of Dialkyl Phosphites and Diphenylphosphine Oxide on the Triple Bond of Dimethyl Acetylenedicarboxylate under Solvent-Free and Microwave Conditions

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Cited by 16 publications
(9 citation statements)
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“…Treatment of 13 with HP­(O)­(OEt) 2 does indeed generate 5 and the vinyl phosphonate (90 °C, 20 h). However, the development of a catalytic process was hindered by the observation that an uncatalyzed double-addition reaction occurs between DMAD and HP­(O)­(OEt) 2 (2 equiv) under the insertion conditions (80 °C, 2 days) . A successful catalytic approach needs to circumvent this background reaction.…”
Section: Resultsmentioning
confidence: 99%
“…Treatment of 13 with HP­(O)­(OEt) 2 does indeed generate 5 and the vinyl phosphonate (90 °C, 20 h). However, the development of a catalytic process was hindered by the observation that an uncatalyzed double-addition reaction occurs between DMAD and HP­(O)­(OEt) 2 (2 equiv) under the insertion conditions (80 °C, 2 days) . A successful catalytic approach needs to circumvent this background reaction.…”
Section: Resultsmentioning
confidence: 99%
“…MW addition was useful to enhance the addition of dialkyl phosphites, ethyl phenyl‐ H ‐phosphinate and diphenylphosphine oxide to the more reactive double‐bond of N ‐phenyl and N ‐methylmaleimide, as well as maleic anhydride . The addition of two equivalents of >P(O)H species to dimethyl acetylenedicarboxylate and analogous derivatives was also studied …”
Section: Reactions Taking Place More Efficiently Under Mw Conditionsmentioning
confidence: 99%
“…Products 39 and 40 were obtained, with one exception, in good yields. Depending on the molar ratio of the reactants and the conditions (temperature and reaction time), the addition of dialkyl phosphites or diphenylphosphine oxide to the triple bond of dimethyl acetylenedicarboxylate resulted in the formation of a comparable mixture of the corresponding monoadduct (41) and bisadduct (42), or the bisadduct (42) as the predominating or exclusive product (Scheme 3.29, Table 3.7) [61].…”
Section: -86%mentioning
confidence: 99%