1955
DOI: 10.1093/ajcn/3.4.298
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Pantothenic Acid Antagonists

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Cited by 6 publications
(17 citation statements)
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“…65 (m, 1H), 1.50 (dd, J = 5.2, 13.9, 1H), 1.30 (t, J = 7.1, 3H), 1.29 (t, J = 7.1, 3H), 1.16 (s, 3H), 0.93 (d, J = 6.6, 3H), 0.85 (t, J = 6.6, 3H). 13 (s, 3H). 13 (R)-diethyl 3-hydroxy-2, 2-dipropylsuccinate (4h) and (R)-diethyl 2, 2-diallyl-3-hydroxysuccinate (4i) were difficult to purify from the reaction mixture because their Rf was very close to that of the starting materials (3h and 3i respectively).…”
Section: Synthesis Of Compoundsmentioning
confidence: 99%
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“…65 (m, 1H), 1.50 (dd, J = 5.2, 13.9, 1H), 1.30 (t, J = 7.1, 3H), 1.29 (t, J = 7.1, 3H), 1.16 (s, 3H), 0.93 (d, J = 6.6, 3H), 0.85 (t, J = 6.6, 3H). 13 (s, 3H). 13 (R)-diethyl 3-hydroxy-2, 2-dipropylsuccinate (4h) and (R)-diethyl 2, 2-diallyl-3-hydroxysuccinate (4i) were difficult to purify from the reaction mixture because their Rf was very close to that of the starting materials (3h and 3i respectively).…”
Section: Synthesis Of Compoundsmentioning
confidence: 99%
“…13 (s, 3H). 13 (R)-diethyl 3-hydroxy-2, 2-dipropylsuccinate (4h) and (R)-diethyl 2, 2-diallyl-3-hydroxysuccinate (4i) were difficult to purify from the reaction mixture because their Rf was very close to that of the starting materials (3h and 3i respectively). A mixture containing some starting materials 3h and 3i was carried over to the next reaction (reduction and selective protection) from where pure 5h and 5i were obtained.…”
Section: Synthesis Of Compoundsmentioning
confidence: 99%
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