1973
DOI: 10.1055/s-1973-22304
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A Mild Transesterification Method

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Cited by 105 publications
(39 citation statements)
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“…JH titers were analyzed on a Trace 2000 series gas chromatograph (GC) coupled to a Finnigan Polaris mass spectrometer detector (MS). An internal standard, JH III ethyl ester, was made from synthetic JH III (Sigma, St. Louis, MO) by using a mild transesteriÞcation method (Mori et al 1973, Liu et al 2004) and quantiÞed on the same GC-MS system (Liu et al 2004). The GC was equipped with a DB-5MS column (30 m by 0.25 mm by 0.25 m, J & W ScientiÞc, Folsom, CA).…”
Section: Methodsmentioning
confidence: 99%
“…JH titers were analyzed on a Trace 2000 series gas chromatograph (GC) coupled to a Finnigan Polaris mass spectrometer detector (MS). An internal standard, JH III ethyl ester, was made from synthetic JH III (Sigma, St. Louis, MO) by using a mild transesteriÞcation method (Mori et al 1973, Liu et al 2004) and quantiÞed on the same GC-MS system (Liu et al 2004). The GC was equipped with a DB-5MS column (30 m by 0.25 mm by 0.25 m, J & W ScientiÞc, Folsom, CA).…”
Section: Methodsmentioning
confidence: 99%
“…4 ) This transesterification is mild enough to prevent the equilibration of the geometry of the C-2 double bond due to enolization of the ester carbonyl group. These ethyl esters (VII) were epoxidized as usual to give another set of JH Tables I and II as expressed in termes of the percentages of larvae molted into larva.…”
Section: Synthesis and Biological Activity Of Jh Analogs With Carbomementioning
confidence: 99%
“…The methyl (12), cyclopentyl (16), and benzyl (17) acetate derivatives were prepared via transesterification [47], by refluxing the ethyl ester 13 in the suitable alcohol in the presence of a catalytic amount of sodium cyanide. The same catalyst was used for aminolysis [48] of 13 with an excess of pyrrolidine at 50 ± 558 to yield the amide 18.…”
mentioning
confidence: 99%