Interaction of C-Alkylsubstituted-1,4,8,11-tetraazacyclotetradeca-4,11-dienes with Carboxylic Acid Halides as a New Method for the Synthesis of C- and N-Acyl-2,3,6,7-tetrahydro-1,4-diazepines

Abstract The reactions of 5,7,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradeca-4,11-diene with acetic and tetrafluorobenzoic acids halides produce C- and N- acyl-substituted 1,4-diazepines. Their structure was characterized by IR, 1Н, and 13С NMR spectroscopy using two-dimensional experiments 1...
Ausführliche Beschreibung

Gespeichert in:

Autor*in:	Anisimova, N. A. [verfasserIn] Melkova, D. A.

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2022

Anmerkung:	© Pleiades Publishing, Ltd. 2022

Übergeordnetes Werk:	Enthalten in: Russian journal of general chemistry - Dordrecht : Springer Science + Business Media B.V., 1996, 92(2022), 12 vom: Dez., Seite 2809-2815
Übergeordnetes Werk:	volume:92 ; year:2022 ; number:12 ; month:12 ; pages:2809-2815

Links:	Volltext

DOI / URN:	10.1134/S1070363222120313

Katalog-ID:	SPR051430363

Internformat


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100	1		\|a Anisimova, N. A. \|e verfasserin \|4 aut
245	1	0	\|a Interaction of C-Alkylsubstituted-1,4,8,11-tetraazacyclotetradeca-4,11-dienes with Carboxylic Acid Halides as a New Method for the Synthesis of C- and N-Acyl-2,3,6,7-tetrahydro-1,4-diazepines
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520			\|a Abstract The reactions of 5,7,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradeca-4,11-diene with acetic and tetrafluorobenzoic acids halides produce C- and N- acyl-substituted 1,4-diazepines. Their structure was characterized by IR, 1Н, and 13С NMR spectroscopy using two-dimensional experiments 1Н–13С HMQC, HMBC, and 1Н–1Н COSY.
700	1		\|a Melkova, D. A. \|4 aut
773	0	8	\|i Enthalten in \|t Russian journal of general chemistry \|d Dordrecht : Springer Science + Business Media B.V., 1996 \|g 92(2022), 12 vom: Dez., Seite 2809-2815 \|w (DE-627)340146834 \|w (DE-600)2065665-8 \|x 1608-3350 \|7 nnns
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912			\|a GBV_ILN_24
912			\|a GBV_ILN_31
912			\|a GBV_ILN_32
912			\|a GBV_ILN_39
912			\|a GBV_ILN_40
912			\|a GBV_ILN_60
912			\|a GBV_ILN_62
912			\|a GBV_ILN_63
912			\|a GBV_ILN_69
912			\|a GBV_ILN_70
912			\|a GBV_ILN_73
912			\|a GBV_ILN_74
912			\|a GBV_ILN_90
912			\|a GBV_ILN_95
912			\|a GBV_ILN_100
912			\|a GBV_ILN_101
912			\|a GBV_ILN_105
912			\|a GBV_ILN_110
912			\|a GBV_ILN_120
912			\|a GBV_ILN_138
912			\|a GBV_ILN_150
912			\|a GBV_ILN_151
912			\|a GBV_ILN_152
912			\|a GBV_ILN_161
912			\|a GBV_ILN_170
912			\|a GBV_ILN_171
912			\|a GBV_ILN_187
912			\|a GBV_ILN_206
912			\|a GBV_ILN_213
912			\|a GBV_ILN_224
912			\|a GBV_ILN_230
912			\|a GBV_ILN_250
912			\|a GBV_ILN_281
912			\|a GBV_ILN_285
912			\|a GBV_ILN_293
912			\|a GBV_ILN_370
912			\|a GBV_ILN_602
912			\|a GBV_ILN_636
912			\|a GBV_ILN_702
912			\|a GBV_ILN_2001
912			\|a GBV_ILN_2003
912			\|a GBV_ILN_2004
912			\|a GBV_ILN_2005
912			\|a GBV_ILN_2006
912			\|a GBV_ILN_2007
912			\|a GBV_ILN_2008
912			\|a GBV_ILN_2009
912			\|a GBV_ILN_2010
912			\|a GBV_ILN_2011
912			\|a GBV_ILN_2014
912			\|a GBV_ILN_2015
912			\|a GBV_ILN_2020
912			\|a GBV_ILN_2021
912			\|a GBV_ILN_2025
912			\|a GBV_ILN_2026
912			\|a GBV_ILN_2027
912			\|a GBV_ILN_2031
912			\|a GBV_ILN_2034
912			\|a GBV_ILN_2037
912			\|a GBV_ILN_2038
912			\|a GBV_ILN_2039
912			\|a GBV_ILN_2044
912			\|a GBV_ILN_2048
912			\|a GBV_ILN_2049
912			\|a GBV_ILN_2050
912			\|a GBV_ILN_2055
912			\|a GBV_ILN_2056
912			\|a GBV_ILN_2057
912			\|a GBV_ILN_2059
912			\|a GBV_ILN_2061
912			\|a GBV_ILN_2064
912			\|a GBV_ILN_2065
912			\|a GBV_ILN_2068
912			\|a GBV_ILN_2088
912			\|a GBV_ILN_2093
912			\|a GBV_ILN_2106
912			\|a GBV_ILN_2107
912			\|a GBV_ILN_2108
912			\|a GBV_ILN_2110
912			\|a GBV_ILN_2111
912			\|a GBV_ILN_2112
912			\|a GBV_ILN_2113
912			\|a GBV_ILN_2118
912			\|a GBV_ILN_2122
912			\|a GBV_ILN_2129
912			\|a GBV_ILN_2143
912			\|a GBV_ILN_2144
912			\|a GBV_ILN_2147
912			\|a GBV_ILN_2148
912			\|a GBV_ILN_2152
912			\|a GBV_ILN_2153
912			\|a GBV_ILN_2188
912			\|a GBV_ILN_2190
912			\|a GBV_ILN_2232
912			\|a GBV_ILN_2336
912			\|a GBV_ILN_2446
912			\|a GBV_ILN_2470
912			\|a GBV_ILN_2472
912			\|a GBV_ILN_2507
912			\|a GBV_ILN_2522
912			\|a GBV_ILN_2548
912			\|a GBV_ILN_4035
912			\|a GBV_ILN_4037
912			\|a GBV_ILN_4046
912			\|a GBV_ILN_4112
912			\|a GBV_ILN_4125
912			\|a GBV_ILN_4126
912			\|a GBV_ILN_4242
912			\|a GBV_ILN_4246
912			\|a GBV_ILN_4249
912			\|a GBV_ILN_4251
912			\|a GBV_ILN_4305
912			\|a GBV_ILN_4306
912			\|a GBV_ILN_4307
912			\|a GBV_ILN_4313
912			\|a GBV_ILN_4322
912			\|a GBV_ILN_4323
912			\|a GBV_ILN_4324
912			\|a GBV_ILN_4325
912			\|a GBV_ILN_4326
912			\|a GBV_ILN_4328
912			\|a GBV_ILN_4333
912			\|a GBV_ILN_4334
912			\|a GBV_ILN_4335
912			\|a GBV_ILN_4336
912			\|a GBV_ILN_4338
912			\|a GBV_ILN_4393
912			\|a GBV_ILN_4700
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952			\|d 92 \|j 2022 \|e 12 \|c 12 \|h 2809-2815

Indexfelder

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allfields	10.1134/S1070363222120313 doi (DE-627)SPR051430363 (SPR)S1070363222120313-e DE-627 ger DE-627 rakwb eng Anisimova, N. A. verfasserin aut Interaction of C-Alkylsubstituted-1,4,8,11-tetraazacyclotetradeca-4,11-dienes with Carboxylic Acid Halides as a New Method for the Synthesis of C- and N-Acyl-2,3,6,7-tetrahydro-1,4-diazepines 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Pleiades Publishing, Ltd. 2022 Abstract The reactions of 5,7,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradeca-4,11-diene with acetic and tetrafluorobenzoic acids halides produce C- and N- acyl-substituted 1,4-diazepines. Their structure was characterized by IR, 1Н, and 13С NMR spectroscopy using two-dimensional experiments 1Н–13С HMQC, HMBC, and 1Н–1Н COSY. Melkova, D. A. aut Enthalten in Russian journal of general chemistry Dordrecht : Springer Science + Business Media B.V., 1996 92(2022), 12 vom: Dez., Seite 2809-2815 (DE-627)340146834 (DE-600)2065665-8 1608-3350 nnns volume:92 year:2022 number:12 month:12 pages:2809-2815 https://dx.doi.org/10.1134/S1070363222120313 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 92 2022 12 12 2809-2815
spelling	10.1134/S1070363222120313 doi (DE-627)SPR051430363 (SPR)S1070363222120313-e DE-627 ger DE-627 rakwb eng Anisimova, N. A. verfasserin aut Interaction of C-Alkylsubstituted-1,4,8,11-tetraazacyclotetradeca-4,11-dienes with Carboxylic Acid Halides as a New Method for the Synthesis of C- and N-Acyl-2,3,6,7-tetrahydro-1,4-diazepines 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Pleiades Publishing, Ltd. 2022 Abstract The reactions of 5,7,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradeca-4,11-diene with acetic and tetrafluorobenzoic acids halides produce C- and N- acyl-substituted 1,4-diazepines. Their structure was characterized by IR, 1Н, and 13С NMR spectroscopy using two-dimensional experiments 1Н–13С HMQC, HMBC, and 1Н–1Н COSY. Melkova, D. A. aut Enthalten in Russian journal of general chemistry Dordrecht : Springer Science + Business Media B.V., 1996 92(2022), 12 vom: Dez., Seite 2809-2815 (DE-627)340146834 (DE-600)2065665-8 1608-3350 nnns volume:92 year:2022 number:12 month:12 pages:2809-2815 https://dx.doi.org/10.1134/S1070363222120313 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 92 2022 12 12 2809-2815
allfields_unstemmed	10.1134/S1070363222120313 doi (DE-627)SPR051430363 (SPR)S1070363222120313-e DE-627 ger DE-627 rakwb eng Anisimova, N. A. verfasserin aut Interaction of C-Alkylsubstituted-1,4,8,11-tetraazacyclotetradeca-4,11-dienes with Carboxylic Acid Halides as a New Method for the Synthesis of C- and N-Acyl-2,3,6,7-tetrahydro-1,4-diazepines 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Pleiades Publishing, Ltd. 2022 Abstract The reactions of 5,7,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradeca-4,11-diene with acetic and tetrafluorobenzoic acids halides produce C- and N- acyl-substituted 1,4-diazepines. Their structure was characterized by IR, 1Н, and 13С NMR spectroscopy using two-dimensional experiments 1Н–13С HMQC, HMBC, and 1Н–1Н COSY. Melkova, D. A. aut Enthalten in Russian journal of general chemistry Dordrecht : Springer Science + Business Media B.V., 1996 92(2022), 12 vom: Dez., Seite 2809-2815 (DE-627)340146834 (DE-600)2065665-8 1608-3350 nnns volume:92 year:2022 number:12 month:12 pages:2809-2815 https://dx.doi.org/10.1134/S1070363222120313 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 92 2022 12 12 2809-2815
allfieldsGer	10.1134/S1070363222120313 doi (DE-627)SPR051430363 (SPR)S1070363222120313-e DE-627 ger DE-627 rakwb eng Anisimova, N. A. verfasserin aut Interaction of C-Alkylsubstituted-1,4,8,11-tetraazacyclotetradeca-4,11-dienes with Carboxylic Acid Halides as a New Method for the Synthesis of C- and N-Acyl-2,3,6,7-tetrahydro-1,4-diazepines 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Pleiades Publishing, Ltd. 2022 Abstract The reactions of 5,7,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradeca-4,11-diene with acetic and tetrafluorobenzoic acids halides produce C- and N- acyl-substituted 1,4-diazepines. Their structure was characterized by IR, 1Н, and 13С NMR spectroscopy using two-dimensional experiments 1Н–13С HMQC, HMBC, and 1Н–1Н COSY. Melkova, D. A. aut Enthalten in Russian journal of general chemistry Dordrecht : Springer Science + Business Media B.V., 1996 92(2022), 12 vom: Dez., Seite 2809-2815 (DE-627)340146834 (DE-600)2065665-8 1608-3350 nnns volume:92 year:2022 number:12 month:12 pages:2809-2815 https://dx.doi.org/10.1134/S1070363222120313 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 92 2022 12 12 2809-2815
allfieldsSound	10.1134/S1070363222120313 doi (DE-627)SPR051430363 (SPR)S1070363222120313-e DE-627 ger DE-627 rakwb eng Anisimova, N. A. verfasserin aut Interaction of C-Alkylsubstituted-1,4,8,11-tetraazacyclotetradeca-4,11-dienes with Carboxylic Acid Halides as a New Method for the Synthesis of C- and N-Acyl-2,3,6,7-tetrahydro-1,4-diazepines 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Pleiades Publishing, Ltd. 2022 Abstract The reactions of 5,7,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradeca-4,11-diene with acetic and tetrafluorobenzoic acids halides produce C- and N- acyl-substituted 1,4-diazepines. Their structure was characterized by IR, 1Н, and 13С NMR spectroscopy using two-dimensional experiments 1Н–13С HMQC, HMBC, and 1Н–1Н COSY. Melkova, D. A. aut Enthalten in Russian journal of general chemistry Dordrecht : Springer Science + Business Media B.V., 1996 92(2022), 12 vom: Dez., Seite 2809-2815 (DE-627)340146834 (DE-600)2065665-8 1608-3350 nnns volume:92 year:2022 number:12 month:12 pages:2809-2815 https://dx.doi.org/10.1134/S1070363222120313 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 92 2022 12 12 2809-2815
language	English
source	Enthalten in Russian journal of general chemistry 92(2022), 12 vom: Dez., Seite 2809-2815 volume:92 year:2022 number:12 month:12 pages:2809-2815
sourceStr	Enthalten in Russian journal of general chemistry 92(2022), 12 vom: Dez., Seite 2809-2815 volume:92 year:2022 number:12 month:12 pages:2809-2815
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container_title	Russian journal of general chemistry
authorswithroles_txt_mv	Anisimova, N. A. @@aut@@ Melkova, D. A. @@aut@@
publishDateDaySort_date	2022-12-01T00:00:00Z
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author	Anisimova, N. A.
spellingShingle	Anisimova, N. A. Interaction of C-Alkylsubstituted-1,4,8,11-tetraazacyclotetradeca-4,11-dienes with Carboxylic Acid Halides as a New Method for the Synthesis of C- and N-Acyl-2,3,6,7-tetrahydro-1,4-diazepines
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topic_title	Interaction of C-Alkylsubstituted-1,4,8,11-tetraazacyclotetradeca-4,11-dienes with Carboxylic Acid Halides as a New Method for the Synthesis of C- and N-Acyl-2,3,6,7-tetrahydro-1,4-diazepines
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title	Interaction of C-Alkylsubstituted-1,4,8,11-tetraazacyclotetradeca-4,11-dienes with Carboxylic Acid Halides as a New Method for the Synthesis of C- and N-Acyl-2,3,6,7-tetrahydro-1,4-diazepines
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title_full	Interaction of C-Alkylsubstituted-1,4,8,11-tetraazacyclotetradeca-4,11-dienes with Carboxylic Acid Halides as a New Method for the Synthesis of C- and N-Acyl-2,3,6,7-tetrahydro-1,4-diazepines
author_sort	Anisimova, N. A.
journal	Russian journal of general chemistry
journalStr	Russian journal of general chemistry
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container_start_page	2809
author_browse	Anisimova, N. A. Melkova, D. A.
container_volume	92
format_se	Elektronische Aufsätze
author-letter	Anisimova, N. A.
doi_str_mv	10.1134/S1070363222120313
title_sort	interaction of c-alkylsubstituted-1,4,8,11-tetraazacyclotetradeca-4,11-dienes with carboxylic acid halides as a new method for the synthesis of c- and n-acyl-2,3,6,7-tetrahydro-1,4-diazepines
title_auth	Interaction of C-Alkylsubstituted-1,4,8,11-tetraazacyclotetradeca-4,11-dienes with Carboxylic Acid Halides as a New Method for the Synthesis of C- and N-Acyl-2,3,6,7-tetrahydro-1,4-diazepines
abstract	Abstract The reactions of 5,7,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradeca-4,11-diene with acetic and tetrafluorobenzoic acids halides produce C- and N- acyl-substituted 1,4-diazepines. Their structure was characterized by IR, 1Н, and 13С NMR spectroscopy using two-dimensional experiments 1Н–13С HMQC, HMBC, and 1Н–1Н COSY. © Pleiades Publishing, Ltd. 2022
abstractGer	Abstract The reactions of 5,7,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradeca-4,11-diene with acetic and tetrafluorobenzoic acids halides produce C- and N- acyl-substituted 1,4-diazepines. Their structure was characterized by IR, 1Н, and 13С NMR spectroscopy using two-dimensional experiments 1Н–13С HMQC, HMBC, and 1Н–1Н COSY. © Pleiades Publishing, Ltd. 2022
abstract_unstemmed	Abstract The reactions of 5,7,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradeca-4,11-diene with acetic and tetrafluorobenzoic acids halides produce C- and N- acyl-substituted 1,4-diazepines. Their structure was characterized by IR, 1Н, and 13С NMR spectroscopy using two-dimensional experiments 1Н–13С HMQC, HMBC, and 1Н–1Н COSY. © Pleiades Publishing, Ltd. 2022
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title_short	Interaction of C-Alkylsubstituted-1,4,8,11-tetraazacyclotetradeca-4,11-dienes with Carboxylic Acid Halides as a New Method for the Synthesis of C- and N-Acyl-2,3,6,7-tetrahydro-1,4-diazepines
url	https://dx.doi.org/10.1134/S1070363222120313
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author2	Melkova, D. A.
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doi_str	10.1134/S1070363222120313
up_date	2024-07-03T21:45:59.696Z
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Interaction of C-Alkylsubstituted-1,4,8,11-tetraazacyclotetradeca-4,11-dienes with Carboxylic Acid Halides as a New Method for the Synthesis of C- and N-Acyl-2,3,6,7-tetrahydro-1,4-diazepines

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