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Paquette, Leo A., Kakihana, Tsuyoshi. (1968) Unsaturated heterocyclic systems. XLIII. The azacyclooctatetraene (azocine) system. Journal Of The American Chemical Society, 90 (14) 3897-3898 doi:10.1021/ja01016a073

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Reference TypeJournal (article/letter/editorial)
TitleUnsaturated heterocyclic systems. XLIII. The azacyclooctatetraene (azocine) system
JournalJournal Of The American Chemical Society
AuthorsPaquette, Leo A.Author
Kakihana, Tsuyoshi.Author
Year1968 (July)Volume90
Issue14
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ja01016a073Search in ResearchGate
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Mindat Ref. ID1298093Long-form Identifiermindat:1:5:1298093:4
GUID0
Full ReferencePaquette, Leo A., Kakihana, Tsuyoshi. (1968) Unsaturated heterocyclic systems. XLIII. The azacyclooctatetraene (azocine) system. Journal Of The American Chemical Society, 90 (14) 3897-3898 doi:10.1021/ja01016a073
Plain TextPaquette, Leo A., Kakihana, Tsuyoshi. (1968) Unsaturated heterocyclic systems. XLIII. The azacyclooctatetraene (azocine) system. Journal Of The American Chemical Society, 90 (14) 3897-3898 doi:10.1021/ja01016a073
In(1968, July) Journal Of The American Chemical Society Vol. 90 (14) American Chemical Society (ACS)

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Paquette, Leo A., Philips, J. Christopher. (1968) Unsaturated heterocyclic systems. XLIV. Concerning azacyclooctatetraene valence tautomerism. Preparation of annelated 7-azabicyclo[4.2.0]octa-2,4,7-trienes. Journal Of The American Chemical Society, 90 (14) 3898-3899 doi:10.1021/ja01016a074
Paquette, Leo A., Hansen, John F., Kakihana, Tsuyoshi (1971) Unsaturated heterocyclic systems. LXXV. Generation and protonation of azocinyl dianions. Journal Of The American Chemical Society, 93 (1) 168-173 doi:10.1021/ja00730a029
Paquette, Leo A., Kakihana, Tsuyoshi (1971) Unsaturated heterocyclic systems. LXXVI. Reactions of azocinyl dianions with nonenolizable ketones and aldehydes. Formation of 2,3-pyridocyclobutenes. Journal Of The American Chemical Society, 93 (1) 174-178 doi:10.1021/ja00730a030
Paquette, Leo A., Kakihana, Tsuyoshi, Hansen, John F., Philips, J. Christopher (1971) Unsaturated heterocyclic systems. LXXIII.pi.-Equivalent heterocyclic congeners of cyclooctatetraene. Synthesis and valance isomerization of 2-alkoxyazocines. Journal Of The American Chemical Society, 93 (1) 152-161 doi:10.1021/ja00730a027
Paquette, Leo A., Anderson, Larry Bernard, Hansen, John F., Kakihana, Tsuyoshi (1971) Unsaturated heterocyclic systems. LXXIV. Electrochemical studies of the reduction of 2-methoxyazocines in aprotic solvents. Comparison with the cyclooctatetraene system. Journal Of The American Chemical Society, 93 (1) 161-167 doi:10.1021/ja00730a028
Paquette, Leo A., Malpass, John R. (1968) Unsaturated heterocyclic systems. XLVIII. Benzazabullvalenes. Synthesis and interconvertibility. Journal Of The American Chemical Society, 90 (25) 7151-7153 doi:10.1021/ja01027a062
Paquette, Leo A., Krow, Grant R. (1968) Unsaturated heterocyclic systems. XLVII. Photochemical transformations of 2-methoxyazabullvalene. Journal Of The American Chemical Society, 90 (25) 7149-7151 doi:10.1021/ja01027a061
Paquette, Leo A., Wise, Lawrence David. (1968) Unsaturated heterocyclic systems. XXXV. Deuterium substitution in the 4H-thiopyran-4-one 1,1-dioxide system. Journal Of The American Chemical Society, 90 (3) 807-808 doi:10.1021/ja01005a055
Paquette, Leo A., Anderson, Larry B., Hansen, John F., Lang, Stanley A., Berk, Howard (1972) Unsaturated heterocyclic systems. LXXXV. Benzoannelation effects on azocine reactivity. Chemical and polarographic reduction of several mono-, di-, and tribenzomethoxyazocines. Journal Of The American Chemical Society, 94 (14) 4907-4915 doi:10.1021/ja00769a020
Paquette, Leo A., Krow, Grant R. (1969) Unsaturated heterocyclic systems. LXII. A synthetic entry into the azasemibullvalene system. Journal Of The American Chemical Society, 91 (22) 6107-6111 doi:10.1021/ja01050a030
Paquette, Leo A., Krow, Grant R., Malpass, John R., Barton, Thomas J. (1968) Unsaturated heterocyclic systems. XLII. Pyrolysis of azabullvalenes and 7-azabicyclo[4.2.2]deca-2,4,7,9-tetraenes. Journal Of The American Chemical Society, 90 (13) 3600-3601 doi:10.1021/ja01015a076
 
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