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Hrnčiar, P., Szémes, F. (1974) Reactions of the 5,7-dioxo-6-phenyl-6,7-dihydro-5H-dibenzo[a,c]cycloheptane anion with monohalohydrocarbons. Collection of Czechoslovak Chemical Communications, 39. 1744-1751 doi:10.1135/cccc19741744

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Reference TypeJournal (article/letter/editorial)
TitleReactions of the 5,7-dioxo-6-phenyl-6,7-dihydro-5H-dibenzo[a,c]cycloheptane anion with monohalohydrocarbons
JournalCollection of Czechoslovak Chemical Communications
AuthorsHrnčiar, P.Author
Szémes, F.Author
Year1974Volume39
PublisherInstitute of Organic Chemistry & Biochemistry
DOIdoi:10.1135/cccc19741744Search in ResearchGate
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Mindat Ref. ID4382831Long-form Identifiermindat:1:5:4382831:9
GUID0
Full ReferenceHrnčiar, P., Szémes, F. (1974) Reactions of the 5,7-dioxo-6-phenyl-6,7-dihydro-5H-dibenzo[a,c]cycloheptane anion with monohalohydrocarbons. Collection of Czechoslovak Chemical Communications, 39. 1744-1751 doi:10.1135/cccc19741744
Plain TextHrnčiar, P., Szémes, F. (1974) Reactions of the 5,7-dioxo-6-phenyl-6,7-dihydro-5H-dibenzo[a,c]cycloheptane anion with monohalohydrocarbons. Collection of Czechoslovak Chemical Communications, 39. 1744-1751 doi:10.1135/cccc19741744
In(1974) Collection of Czechoslovak Chemical Communications Vol. 39. Institute of Organic Chemistry & Biochemistry

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Szémes, F., Hrnčiar, P. (1974) Reactions of 6,7-dihydro-5H-dibenzo[a,c]cyclohepten-5,7-dione with aromatic aldehydes. Collection of Czechoslovak Chemical Communications, 39. 3720-3727 doi:10.1135/cccc19743720
HRNCIAR, P., SZEMES, F. (1974) ChemInform Abstract: REACTIONS OF THE 5,7-DIOXO-6-PHENYL-6,7-DIHYDRO-5H-DIBENZO(A,C)CYCLOHEPTENE ANION WITH MONOHALOHYDROCARBONS. Chemischer Informationsdienst, 5 (40) doi:10.1002/chin.197440178
Zacharová-Kalavská, D., Perjéssy, A, Szémes, F., Hrnčiar, P. (1975) Electroreduction of the enolate-anions of some 5,7-dioxo-6,7-dihydro-5H-dibenzo[a,c]cycloheptene derivatives. The infrared spectra and structures of 5-oxo-7-hydroxy-6,7-dihydro-5H-dibenzo[a,c]cycloheptenes. Collection of Czechoslovak Chemical Communications, 40. 137-141 doi:10.1135/cccc19750137
Nedev, Hinyu N., Stoyanov, Neiko M., Minchev, Stoyan, Aleksiev, Boris V. (1992) Synthesis of 5,7-Dioxo-6-halogenophenyl-6,7-dihydro-5H-dibenzo[a,c]cycloheptene Derivatives. Collection of Czechoslovak Chemical Communications, 57. 1081-1084 doi:10.1135/cccc19921081
ZACHAROVA-KALAVSKA, D., PERJESSY, A., SZEMES, F., HRNCIAR, P. (1975) ChemInform Abstract: ELECTROREDUCTION OF THE ENOLATE-ANIONS OF SOME 5,7-DIOXO-6,7-DIHYDRO-5H-DIBENZO(A,C)CYCLOHEPTEN DERIVATIVES, THE INFRARED SPECTRA AND STRUCTURES OF 5-OXO-7-HYDROXY-6,7-DIHYDRO-5H-DIBENZO(A,C)CYCLOHEPTENES. Chemischer Informationsdienst, 6 (14) doi:10.1002/chin.197514200
SZEMES, F., HRNCIAR, P. (1975) ChemInform Abstract: REACTIONS OF 6,7-DIHYDRO-5H-DIBENZO(A,C)CYCLOHEPTEN-5,7-DIONE WITH AROMATIC ALDEHYDES. Chemischer Informationsdienst, 6 (10) doi:10.1002/chin.197510210
RIED, WALTER, CONTE, RALF (1971) ChemInform Abstract: SYNTHESE UND RK. DES 5,7-DIOXO-6,7-DIHYDRO-5H-DIBENZO(A,C)CYCLOHEPTENS. Chemischer Informationsdienst. Organische Chemie, 2. doi:10.1002/chin.197131285
Hrnčiar, P., Szémes, F. (1971) On phthalides and indandiones. XXXVIII. Alkylation of 2-(1-X-2-naphthyl)-1,3-indandione in ethanol and in dimethylformamide. Collection of Czechoslovak Chemical Communications, 36. 1843-1852 doi:10.1135/cccc19711843
RIED, WALTER, CONTE, RALF (1972) ChemInform Abstract: SYNTH. UND RK. DES 5,7-DIOXO-6,7-DIHYDRO-5H-DIBENZO(A,C)CYCLOHEPTENS 2. MITT. RINGVERENGUNGEN AM DIBENZO(A,C)CYCLOHEPTEN-SYST. Chemischer Informationsdienst, 3 (17) doi:10.1002/chin.197217191
RIED, WALTER, CONTE, RALF (1972) ChemInform Abstract: SYNTH. UND RK. DES 5,7-DIOXO-6,7-DIHYDRO-5H-DIBENZO(A,C)CYCLOHEPTANS 3. MITT. SYNTH. VON DIBENZO(A,C)TROPYLIUM-, AZAAZULENIUMSALZEN UND AZAAZULENEN. Chemischer Informationsdienst, 3 (23) doi:10.1002/chin.197223287
Perjéssy, A., Temkovitz, P., Hrnčiar, P. (1976) C=O stretching vibrations of 5,6-dihydro-4,7-dithia-1,3-indanedione derivatives. Collection of Czechoslovak Chemical Communications, 41. 2904-2910 doi:10.1135/cccc19762904
 
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