1944
DOI: 10.1021/ja01236a034
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Cleavage of Trigonelline

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1946
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Cited by 6 publications
(5 citation statements)
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“…The use of two complementary methods to measure these data demonstrates reliability. Literature data for DMA includes two normal boiling points, the first of which (403.2 K at 101.3 kPa) 19 is in good agreement with our data, but the other (365.2 K at 101.3 kPa) 20 indicates a significantly lower boiling temperature, suggesting that it might have been measured at reduced pressure. The third data point (337.7 K at 13.3 kPa) 21 appears to be a reduced pressure boiling point and is at variance with our data by approximately 7 %.…”
Section: ■ Discussionsupporting
confidence: 89%
“…The use of two complementary methods to measure these data demonstrates reliability. Literature data for DMA includes two normal boiling points, the first of which (403.2 K at 101.3 kPa) 19 is in good agreement with our data, but the other (365.2 K at 101.3 kPa) 20 indicates a significantly lower boiling temperature, suggesting that it might have been measured at reduced pressure. The third data point (337.7 K at 13.3 kPa) 21 appears to be a reduced pressure boiling point and is at variance with our data by approximately 7 %.…”
Section: ■ Discussionsupporting
confidence: 89%
“…At present, there have been no studies on the synthesis of diphenylsulfone‐containing POSS and the impact of sulfone on the POSS thermal stability. Sulfones are useful intermediates in a wide range of fields, including agrochemicals, pharmaceuticals, and polymers . Diarylsulfones are widely used synthons for synthetic organic chemists, and they have many industrial applications …”
Section: Introductionmentioning
confidence: 99%
“…2-(Dialkylamino)ethanethiols of general formula R 1 R 2 NCH 2 CH 2 SH are possible to prepare by the three general methods. The first one involves the reaction of 2-(dialkylamino)ethyl halides with the hydrosulfides of the alkali metals 6,7 . Another method is based on the nucleophilic substitution of the 2-(dialkylamino)ethyl halides with thiourea followed by an alkaline hydrolysis of the isothiouronium salts 8,9 and the last method is the mercaptoethylation of the primary and the secondary amines with ethylene sulfide [10][11][12] or other mercaptoethylating agents such as ethyl 2-hydroxyethylthiolcarbonate [13][14][15] , ethyl 2-mercaptoethylcarbonate [13][14][15] and ethylene monothiolcarbonate 16 .…”
Section: Introductionmentioning
confidence: 99%