Microwave Assisted Synthesis of Novel 1,2,3,4-Tetrahydrocarbazolyl thiazolidin-4-ones and Azetidin-2-ones and its Biological Behavior

A new family of 1,2,3,4 – tetrahydrocarbazolyl thiazolidin-4-ones (4a-e) and 1,2,3,4–tetrahydrocarbazolyl azetidin-2-ones (5a-e) were individually derived using N-[(α-substituted bezylidenehydrazino) acetyl] -1,2,3,4-tetra-hydrocarbazoles 3a-e by cyclization with thioglycolic acid and chloro- acetyl...
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Autor*in:	T. Surendiran [verfasserIn] S. Balasubramanian [verfasserIn] Sivaraj D. [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2009

Übergeordnetes Werk:	In: E-Journal of Chemistry - Hindawi Limited, 2016, 6(2009), S1, Seite S374-S380
Übergeordnetes Werk:	volume:6 ; year:2009 ; number:S1 ; pages:S374-S380

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc Journal toc

DOI / URN:	10.1155/2009/424172

Katalog-ID:	DOAJ005757797

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912			\|a GBV_ILN_206
912			\|a GBV_ILN_213
912			\|a GBV_ILN_224
912			\|a GBV_ILN_230
912			\|a GBV_ILN_285
912			\|a GBV_ILN_293
912			\|a GBV_ILN_602
912			\|a GBV_ILN_636
912			\|a GBV_ILN_2004
912			\|a GBV_ILN_2005
912			\|a GBV_ILN_2006
912			\|a GBV_ILN_2007
912			\|a GBV_ILN_2009
912			\|a GBV_ILN_2010
912			\|a GBV_ILN_2011
912			\|a GBV_ILN_2014
912			\|a GBV_ILN_2026
912			\|a GBV_ILN_2034
912			\|a GBV_ILN_2037
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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_2068
912			\|a GBV_ILN_2088
912			\|a GBV_ILN_2106
912			\|a GBV_ILN_2108
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912			\|a GBV_ILN_2111
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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_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_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_4367
912			\|a GBV_ILN_4700
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Indexfelder

author_variant	t s ts s b sb s d sd
matchkey_str	article:20909810:2009----::irwvassesnhssfoe13ttayrcraoytizldnoeadztdn
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publishDate	2009
allfields	10.1155/2009/424172 doi (DE-627)DOAJ005757797 (DE-599)DOAJd14dda4d546a4366a7ce7e81b028d69c DE-627 ger DE-627 rakwb eng QD1-999 T. Surendiran verfasserin aut Microwave Assisted Synthesis of Novel 1,2,3,4-Tetrahydrocarbazolyl thiazolidin-4-ones and Azetidin-2-ones and its Biological Behavior 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier A new family of 1,2,3,4 – tetrahydrocarbazolyl thiazolidin-4-ones (4a-e) and 1,2,3,4–tetrahydrocarbazolyl azetidin-2-ones (5a-e) were individually derived using N-[(α-substituted bezylidenehydrazino) acetyl] -1,2,3,4-tetra-hydrocarbazoles 3a-e by cyclization with thioglycolic acid and chloro- acetylchloride respectively. The compounds (3a-e) were prepared by condensation of N-(hydrazinoacetyl) 1,2,3,4-tetrahydrocarbazole (2) with a series of aldehydes. The compound 2 was obtained by the hydrazinolysis of N-(chloroacetyl)-1,2,3,4-tetrahydrocarbazole (1). These products were characterized by IR, NMR, MASS spectra and by elemental analysis. All the titled compounds (4a-e) and 5(a-e) were screened for antibacterial and antifungal activities. Chemistry S. Balasubramanian verfasserin aut Sivaraj D. verfasserin aut In E-Journal of Chemistry Hindawi Limited, 2016 6(2009), S1, Seite S374-S380 (DE-627)548128820 (DE-600)2393625-3 20909810 nnns volume:6 year:2009 number:S1 pages:S374-S380 https://doi.org/10.1155/2009/424172 kostenfrei https://doaj.org/article/d14dda4d546a4366a7ce7e81b028d69c kostenfrei http://dx.doi.org/10.1155/2009/424172 kostenfrei https://doaj.org/toc/0973-4945 Journal toc kostenfrei https://doaj.org/toc/2090-9810 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2026 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 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_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 6 2009 S1 S374-S380
spelling	10.1155/2009/424172 doi (DE-627)DOAJ005757797 (DE-599)DOAJd14dda4d546a4366a7ce7e81b028d69c DE-627 ger DE-627 rakwb eng QD1-999 T. Surendiran verfasserin aut Microwave Assisted Synthesis of Novel 1,2,3,4-Tetrahydrocarbazolyl thiazolidin-4-ones and Azetidin-2-ones and its Biological Behavior 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier A new family of 1,2,3,4 – tetrahydrocarbazolyl thiazolidin-4-ones (4a-e) and 1,2,3,4–tetrahydrocarbazolyl azetidin-2-ones (5a-e) were individually derived using N-[(α-substituted bezylidenehydrazino) acetyl] -1,2,3,4-tetra-hydrocarbazoles 3a-e by cyclization with thioglycolic acid and chloro- acetylchloride respectively. The compounds (3a-e) were prepared by condensation of N-(hydrazinoacetyl) 1,2,3,4-tetrahydrocarbazole (2) with a series of aldehydes. The compound 2 was obtained by the hydrazinolysis of N-(chloroacetyl)-1,2,3,4-tetrahydrocarbazole (1). These products were characterized by IR, NMR, MASS spectra and by elemental analysis. All the titled compounds (4a-e) and 5(a-e) were screened for antibacterial and antifungal activities. Chemistry S. Balasubramanian verfasserin aut Sivaraj D. verfasserin aut In E-Journal of Chemistry Hindawi Limited, 2016 6(2009), S1, Seite S374-S380 (DE-627)548128820 (DE-600)2393625-3 20909810 nnns volume:6 year:2009 number:S1 pages:S374-S380 https://doi.org/10.1155/2009/424172 kostenfrei https://doaj.org/article/d14dda4d546a4366a7ce7e81b028d69c kostenfrei http://dx.doi.org/10.1155/2009/424172 kostenfrei https://doaj.org/toc/0973-4945 Journal toc kostenfrei https://doaj.org/toc/2090-9810 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2026 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 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_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 6 2009 S1 S374-S380
allfields_unstemmed	10.1155/2009/424172 doi (DE-627)DOAJ005757797 (DE-599)DOAJd14dda4d546a4366a7ce7e81b028d69c DE-627 ger DE-627 rakwb eng QD1-999 T. Surendiran verfasserin aut Microwave Assisted Synthesis of Novel 1,2,3,4-Tetrahydrocarbazolyl thiazolidin-4-ones and Azetidin-2-ones and its Biological Behavior 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier A new family of 1,2,3,4 – tetrahydrocarbazolyl thiazolidin-4-ones (4a-e) and 1,2,3,4–tetrahydrocarbazolyl azetidin-2-ones (5a-e) were individually derived using N-[(α-substituted bezylidenehydrazino) acetyl] -1,2,3,4-tetra-hydrocarbazoles 3a-e by cyclization with thioglycolic acid and chloro- acetylchloride respectively. The compounds (3a-e) were prepared by condensation of N-(hydrazinoacetyl) 1,2,3,4-tetrahydrocarbazole (2) with a series of aldehydes. The compound 2 was obtained by the hydrazinolysis of N-(chloroacetyl)-1,2,3,4-tetrahydrocarbazole (1). These products were characterized by IR, NMR, MASS spectra and by elemental analysis. All the titled compounds (4a-e) and 5(a-e) were screened for antibacterial and antifungal activities. Chemistry S. Balasubramanian verfasserin aut Sivaraj D. verfasserin aut In E-Journal of Chemistry Hindawi Limited, 2016 6(2009), S1, Seite S374-S380 (DE-627)548128820 (DE-600)2393625-3 20909810 nnns volume:6 year:2009 number:S1 pages:S374-S380 https://doi.org/10.1155/2009/424172 kostenfrei https://doaj.org/article/d14dda4d546a4366a7ce7e81b028d69c kostenfrei http://dx.doi.org/10.1155/2009/424172 kostenfrei https://doaj.org/toc/0973-4945 Journal toc kostenfrei https://doaj.org/toc/2090-9810 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2026 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 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_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 6 2009 S1 S374-S380
allfieldsGer	10.1155/2009/424172 doi (DE-627)DOAJ005757797 (DE-599)DOAJd14dda4d546a4366a7ce7e81b028d69c DE-627 ger DE-627 rakwb eng QD1-999 T. Surendiran verfasserin aut Microwave Assisted Synthesis of Novel 1,2,3,4-Tetrahydrocarbazolyl thiazolidin-4-ones and Azetidin-2-ones and its Biological Behavior 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier A new family of 1,2,3,4 – tetrahydrocarbazolyl thiazolidin-4-ones (4a-e) and 1,2,3,4–tetrahydrocarbazolyl azetidin-2-ones (5a-e) were individually derived using N-[(α-substituted bezylidenehydrazino) acetyl] -1,2,3,4-tetra-hydrocarbazoles 3a-e by cyclization with thioglycolic acid and chloro- acetylchloride respectively. The compounds (3a-e) were prepared by condensation of N-(hydrazinoacetyl) 1,2,3,4-tetrahydrocarbazole (2) with a series of aldehydes. The compound 2 was obtained by the hydrazinolysis of N-(chloroacetyl)-1,2,3,4-tetrahydrocarbazole (1). These products were characterized by IR, NMR, MASS spectra and by elemental analysis. All the titled compounds (4a-e) and 5(a-e) were screened for antibacterial and antifungal activities. Chemistry S. Balasubramanian verfasserin aut Sivaraj D. verfasserin aut In E-Journal of Chemistry Hindawi Limited, 2016 6(2009), S1, Seite S374-S380 (DE-627)548128820 (DE-600)2393625-3 20909810 nnns volume:6 year:2009 number:S1 pages:S374-S380 https://doi.org/10.1155/2009/424172 kostenfrei https://doaj.org/article/d14dda4d546a4366a7ce7e81b028d69c kostenfrei http://dx.doi.org/10.1155/2009/424172 kostenfrei https://doaj.org/toc/0973-4945 Journal toc kostenfrei https://doaj.org/toc/2090-9810 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2026 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 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_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 6 2009 S1 S374-S380
allfieldsSound	10.1155/2009/424172 doi (DE-627)DOAJ005757797 (DE-599)DOAJd14dda4d546a4366a7ce7e81b028d69c DE-627 ger DE-627 rakwb eng QD1-999 T. Surendiran verfasserin aut Microwave Assisted Synthesis of Novel 1,2,3,4-Tetrahydrocarbazolyl thiazolidin-4-ones and Azetidin-2-ones and its Biological Behavior 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier A new family of 1,2,3,4 – tetrahydrocarbazolyl thiazolidin-4-ones (4a-e) and 1,2,3,4–tetrahydrocarbazolyl azetidin-2-ones (5a-e) were individually derived using N-[(α-substituted bezylidenehydrazino) acetyl] -1,2,3,4-tetra-hydrocarbazoles 3a-e by cyclization with thioglycolic acid and chloro- acetylchloride respectively. The compounds (3a-e) were prepared by condensation of N-(hydrazinoacetyl) 1,2,3,4-tetrahydrocarbazole (2) with a series of aldehydes. The compound 2 was obtained by the hydrazinolysis of N-(chloroacetyl)-1,2,3,4-tetrahydrocarbazole (1). These products were characterized by IR, NMR, MASS spectra and by elemental analysis. All the titled compounds (4a-e) and 5(a-e) were screened for antibacterial and antifungal activities. Chemistry S. Balasubramanian verfasserin aut Sivaraj D. verfasserin aut In E-Journal of Chemistry Hindawi Limited, 2016 6(2009), S1, Seite S374-S380 (DE-627)548128820 (DE-600)2393625-3 20909810 nnns volume:6 year:2009 number:S1 pages:S374-S380 https://doi.org/10.1155/2009/424172 kostenfrei https://doaj.org/article/d14dda4d546a4366a7ce7e81b028d69c kostenfrei http://dx.doi.org/10.1155/2009/424172 kostenfrei https://doaj.org/toc/0973-4945 Journal toc kostenfrei https://doaj.org/toc/2090-9810 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ SSG-OLC-PHA GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_636 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2026 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 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_2068 GBV_ILN_2088 GBV_ILN_2106 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2118 GBV_ILN_2122 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 6 2009 S1 S374-S380
language	English
source	In E-Journal of Chemistry 6(2009), S1, Seite S374-S380 volume:6 year:2009 number:S1 pages:S374-S380
sourceStr	In E-Journal of Chemistry 6(2009), S1, Seite S374-S380 volume:6 year:2009 number:S1 pages:S374-S380
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	Chemistry
isfreeaccess_bool	true
container_title	E-Journal of Chemistry
authorswithroles_txt_mv	T. Surendiran @@aut@@ S. Balasubramanian @@aut@@ Sivaraj D. @@aut@@
publishDateDaySort_date	2009-01-01T00:00:00Z
hierarchy_top_id	548128820
id	DOAJ005757797
language_de	englisch
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callnumber-first	Q - Science
author	T. Surendiran
spellingShingle	T. Surendiran misc QD1-999 misc Chemistry Microwave Assisted Synthesis of Novel 1,2,3,4-Tetrahydrocarbazolyl thiazolidin-4-ones and Azetidin-2-ones and its Biological Behavior
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topic_title	QD1-999 Microwave Assisted Synthesis of Novel 1,2,3,4-Tetrahydrocarbazolyl thiazolidin-4-ones and Azetidin-2-ones and its Biological Behavior
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title	Microwave Assisted Synthesis of Novel 1,2,3,4-Tetrahydrocarbazolyl thiazolidin-4-ones and Azetidin-2-ones and its Biological Behavior
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title_full	Microwave Assisted Synthesis of Novel 1,2,3,4-Tetrahydrocarbazolyl thiazolidin-4-ones and Azetidin-2-ones and its Biological Behavior
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author_browse	T. Surendiran S. Balasubramanian Sivaraj D.
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title_sort	microwave assisted synthesis of novel 1,2,3,4-tetrahydrocarbazolyl thiazolidin-4-ones and azetidin-2-ones and its biological behavior
callnumber	QD1-999
title_auth	Microwave Assisted Synthesis of Novel 1,2,3,4-Tetrahydrocarbazolyl thiazolidin-4-ones and Azetidin-2-ones and its Biological Behavior
abstract	A new family of 1,2,3,4 – tetrahydrocarbazolyl thiazolidin-4-ones (4a-e) and 1,2,3,4–tetrahydrocarbazolyl azetidin-2-ones (5a-e) were individually derived using N-[(α-substituted bezylidenehydrazino) acetyl] -1,2,3,4-tetra-hydrocarbazoles 3a-e by cyclization with thioglycolic acid and chloro- acetylchloride respectively. The compounds (3a-e) were prepared by condensation of N-(hydrazinoacetyl) 1,2,3,4-tetrahydrocarbazole (2) with a series of aldehydes. The compound 2 was obtained by the hydrazinolysis of N-(chloroacetyl)-1,2,3,4-tetrahydrocarbazole (1). These products were characterized by IR, NMR, MASS spectra and by elemental analysis. All the titled compounds (4a-e) and 5(a-e) were screened for antibacterial and antifungal activities.
abstractGer	A new family of 1,2,3,4 – tetrahydrocarbazolyl thiazolidin-4-ones (4a-e) and 1,2,3,4–tetrahydrocarbazolyl azetidin-2-ones (5a-e) were individually derived using N-[(α-substituted bezylidenehydrazino) acetyl] -1,2,3,4-tetra-hydrocarbazoles 3a-e by cyclization with thioglycolic acid and chloro- acetylchloride respectively. The compounds (3a-e) were prepared by condensation of N-(hydrazinoacetyl) 1,2,3,4-tetrahydrocarbazole (2) with a series of aldehydes. The compound 2 was obtained by the hydrazinolysis of N-(chloroacetyl)-1,2,3,4-tetrahydrocarbazole (1). These products were characterized by IR, NMR, MASS spectra and by elemental analysis. All the titled compounds (4a-e) and 5(a-e) were screened for antibacterial and antifungal activities.
abstract_unstemmed	A new family of 1,2,3,4 – tetrahydrocarbazolyl thiazolidin-4-ones (4a-e) and 1,2,3,4–tetrahydrocarbazolyl azetidin-2-ones (5a-e) were individually derived using N-[(α-substituted bezylidenehydrazino) acetyl] -1,2,3,4-tetra-hydrocarbazoles 3a-e by cyclization with thioglycolic acid and chloro- acetylchloride respectively. The compounds (3a-e) were prepared by condensation of N-(hydrazinoacetyl) 1,2,3,4-tetrahydrocarbazole (2) with a series of aldehydes. The compound 2 was obtained by the hydrazinolysis of N-(chloroacetyl)-1,2,3,4-tetrahydrocarbazole (1). These products were characterized by IR, NMR, MASS spectra and by elemental analysis. All the titled compounds (4a-e) and 5(a-e) were screened for antibacterial and antifungal activities.
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title_short	Microwave Assisted Synthesis of Novel 1,2,3,4-Tetrahydrocarbazolyl thiazolidin-4-ones and Azetidin-2-ones and its Biological Behavior
url	https://doi.org/10.1155/2009/424172 https://doaj.org/article/d14dda4d546a4366a7ce7e81b028d69c http://dx.doi.org/10.1155/2009/424172 https://doaj.org/toc/0973-4945 https://doaj.org/toc/2090-9810
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Microwave Assisted Synthesis of Novel 1,2,3,4-Tetrahydrocarbazolyl thiazolidin-4-ones and Azetidin-2-ones and its Biological Behavior

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