1943
DOI: 10.1002/cber.19430760608
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Beitrag zur Kenntnis der Reaktionsfähigkeit höherer Alkylhalogenide

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1944
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Cited by 28 publications
(2 citation statements)
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“…The 2-alkanols synthesized and their melting points and boiling points are as follows: 2-tridecanol, bp 115-116 °C (0.2 mm); 2-tetradecanol, bp 120-122 °C (0.2 mm); 2pentadecanol, bp 124-126 °C (0.2 mm); 2-hexadecanol, bp 129-132 °C (0.2 mm) [lit. bp 135 °C (1 mm); Asinger and Eckoldt, 1943], mp 42-43 °C (lit. mp 42.2-45 °C; Breusch and Sokullu, 1953); 2-heptadecanol, bp 135-138 °C (0.2 mm), mp 46-47 °C (lit.…”
mentioning
confidence: 99%
“…The 2-alkanols synthesized and their melting points and boiling points are as follows: 2-tridecanol, bp 115-116 °C (0.2 mm); 2-tetradecanol, bp 120-122 °C (0.2 mm); 2pentadecanol, bp 124-126 °C (0.2 mm); 2-hexadecanol, bp 129-132 °C (0.2 mm) [lit. bp 135 °C (1 mm); Asinger and Eckoldt, 1943], mp 42-43 °C (lit. mp 42.2-45 °C; Breusch and Sokullu, 1953); 2-heptadecanol, bp 135-138 °C (0.2 mm), mp 46-47 °C (lit.…”
mentioning
confidence: 99%
“…In both series the rate becomes constant with the third and second member, respectively. The n-propyl and higher ketones (17)(18)(19)(20)(21)(22)(23)(24)(25)(26)(27) have the same rate. The above order of reactivity holds true for all of the branched homologous series shown in Table I, the isopropyl ketones (28-34) serving as an example.…”
mentioning
confidence: 99%