Anomale Michaelis-Becker-Reaktion: 1-PhenyIethan-1,2,2-trisphosphonsäure und ihre Ester / Anomalous Michaelis-Becker Reaction: 1-Phenylethan-1,2,2-triphosphonic Acid and their Esters
1985 ◽
Vol 40
(9)
◽
pp. 1152-1156
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Sodium dialkylphosphite reacts with trichlorovinylbenzene to yield in an one-batch procedure 1-phenyl-1,2,2-ethanetrisphosphonic acid hexaalkyl esters. A carbanionic intermediate of an “anomalous Michaelis-Becker reaction” is deduced. Acidolysis of esters leads to the parent trisphosphonic acids. NMR param eters of this acid are strongly influenced by protolytic equilibrium.
2020 ◽
Vol 94
(10)
◽
pp. 2030-2033
2013 ◽
Vol 25
(12)
◽
pp. 831-841
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2018 ◽
Vol 171
◽
pp. 530-537
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Keyword(s):
Algorithm for Calculating the Protolytic Equilibrium Constants of Organic Acids in Isopropyl Alcohol
2021 ◽
Vol 95
(9)
◽
pp. 1826-1830
1994 ◽
Vol 12
(4)
◽
pp. 329-356
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Keyword(s):