J. Am. Chem. Soc.
 1961
DOI: 10.1021/ja01464a022
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Kinetics of Thiosemicarbazone Formation of Some Alkylbutyrophenones

Jane L. Maxwell1,
M. Joanne Brownlee2,
Maretta P. Holden3
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“…i-C,14 + C414 = -> C122<14>® (9) Therefore, the fragments from cracking at the higher olefin addition rate would also show a slight increase in their radioactive content. Formation of nonanes during alkylation is most probably the result of secondary reactions.…”
Section: Methodsmentioning
confidence: 99%

Ionic Reactions Occurring During Sulfuric Acid Catalyzed Alkylation. II. Alkylation of Isobutane with C14-Labeled Butenes

Hofmann1,
Schriesheim2
1962
J. Am. Chem. Soc.
24
1
11
0
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“…i-C,14 + C414 = -> C122<14>® (9) Therefore, the fragments from cracking at the higher olefin addition rate would also show a slight increase in their radioactive content. Formation of nonanes during alkylation is most probably the result of secondary reactions.…”
Section: Methodsmentioning
confidence: 99%

Ionic Reactions Occurring During Sulfuric Acid Catalyzed Alkylation. II. Alkylation of Isobutane with C14-Labeled Butenes

Hofmann1,
Schriesheim2
1962
J. Am. Chem. Soc.
24
1
11
0
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Carbon—nitrogen and nitrogen—nitrogen double bond condensation reactions

Sollenberger
1
,
Martin
2
1968
PATAI'S Chemistry of Functional Groups
11
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4
0
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