Alkylation of oxytriazene oxide salts with 2-(chloromethoxy)diazene 1-oxide derivatives

Abstract A general synthesis of 2-chloromethoxy-1-diazene oxides from their salts was developed. Alkylation of the sodium salts of oxytriazene oxides with 2-chloromethoxy-1-diazene oxides gave hitherto unknown compounds bearing the oxydiazene oxide and oxytriazene oxide units bridged by the methylen...
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Gespeichert in:

Autor*in:	Gordeev, P. B. [verfasserIn] Smirnov, G. A.

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2023

Anmerkung:	© Springer Science+Business Media LLC 2023

Übergeordnetes Werk:	Enthalten in: Russian chemical bulletin - New York, NY [u.a.] : Consultants Bureau, 1952, 72(2023), 7 vom: Juli, Seite 1584-1590
Übergeordnetes Werk:	volume:72 ; year:2023 ; number:7 ; month:07 ; pages:1584-1590

Links:	Volltext

DOI / URN:	10.1007/s11172-023-3937-4

Katalog-ID:	SPR052616967

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520			\|a Abstract A general synthesis of 2-chloromethoxy-1-diazene oxides from their salts was developed. Alkylation of the sodium salts of oxytriazene oxides with 2-chloromethoxy-1-diazene oxides gave hitherto unknown compounds bearing the oxydiazene oxide and oxytriazene oxide units bridged by the methylene group via the oxygen atoms. The synthesized compounds are of interest as potential nitric oxide donors in living organisms.
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912			\|a GBV_ILN_2037
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allfields	10.1007/s11172-023-3937-4 doi (DE-627)SPR052616967 (SPR)s11172-023-3937-4-e DE-627 ger DE-627 rakwb eng Gordeev, P. B. verfasserin aut Alkylation of oxytriazene oxide salts with 2-(chloromethoxy)diazene 1-oxide derivatives 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer Science+Business Media LLC 2023 Abstract A general synthesis of 2-chloromethoxy-1-diazene oxides from their salts was developed. Alkylation of the sodium salts of oxytriazene oxides with 2-chloromethoxy-1-diazene oxides gave hitherto unknown compounds bearing the oxydiazene oxide and oxytriazene oxide units bridged by the methylene group via the oxygen atoms. The synthesized compounds are of interest as potential nitric oxide donors in living organisms. Smirnov, G. A. aut Enthalten in Russian chemical bulletin New York, NY [u.a.] : Consultants Bureau, 1952 72(2023), 7 vom: Juli, Seite 1584-1590 (DE-627)325573417 (DE-600)2037677-7 1573-9171 nnns volume:72 year:2023 number:7 month:07 pages:1584-1590 https://dx.doi.org/10.1007/s11172-023-3937-4 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_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 72 2023 7 07 1584-1590
spelling	10.1007/s11172-023-3937-4 doi (DE-627)SPR052616967 (SPR)s11172-023-3937-4-e DE-627 ger DE-627 rakwb eng Gordeev, P. B. verfasserin aut Alkylation of oxytriazene oxide salts with 2-(chloromethoxy)diazene 1-oxide derivatives 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer Science+Business Media LLC 2023 Abstract A general synthesis of 2-chloromethoxy-1-diazene oxides from their salts was developed. Alkylation of the sodium salts of oxytriazene oxides with 2-chloromethoxy-1-diazene oxides gave hitherto unknown compounds bearing the oxydiazene oxide and oxytriazene oxide units bridged by the methylene group via the oxygen atoms. The synthesized compounds are of interest as potential nitric oxide donors in living organisms. Smirnov, G. A. aut Enthalten in Russian chemical bulletin New York, NY [u.a.] : Consultants Bureau, 1952 72(2023), 7 vom: Juli, Seite 1584-1590 (DE-627)325573417 (DE-600)2037677-7 1573-9171 nnns volume:72 year:2023 number:7 month:07 pages:1584-1590 https://dx.doi.org/10.1007/s11172-023-3937-4 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_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 72 2023 7 07 1584-1590
allfields_unstemmed	10.1007/s11172-023-3937-4 doi (DE-627)SPR052616967 (SPR)s11172-023-3937-4-e DE-627 ger DE-627 rakwb eng Gordeev, P. B. verfasserin aut Alkylation of oxytriazene oxide salts with 2-(chloromethoxy)diazene 1-oxide derivatives 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer Science+Business Media LLC 2023 Abstract A general synthesis of 2-chloromethoxy-1-diazene oxides from their salts was developed. Alkylation of the sodium salts of oxytriazene oxides with 2-chloromethoxy-1-diazene oxides gave hitherto unknown compounds bearing the oxydiazene oxide and oxytriazene oxide units bridged by the methylene group via the oxygen atoms. The synthesized compounds are of interest as potential nitric oxide donors in living organisms. Smirnov, G. A. aut Enthalten in Russian chemical bulletin New York, NY [u.a.] : Consultants Bureau, 1952 72(2023), 7 vom: Juli, Seite 1584-1590 (DE-627)325573417 (DE-600)2037677-7 1573-9171 nnns volume:72 year:2023 number:7 month:07 pages:1584-1590 https://dx.doi.org/10.1007/s11172-023-3937-4 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_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 72 2023 7 07 1584-1590
allfieldsGer	10.1007/s11172-023-3937-4 doi (DE-627)SPR052616967 (SPR)s11172-023-3937-4-e DE-627 ger DE-627 rakwb eng Gordeev, P. B. verfasserin aut Alkylation of oxytriazene oxide salts with 2-(chloromethoxy)diazene 1-oxide derivatives 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer Science+Business Media LLC 2023 Abstract A general synthesis of 2-chloromethoxy-1-diazene oxides from their salts was developed. Alkylation of the sodium salts of oxytriazene oxides with 2-chloromethoxy-1-diazene oxides gave hitherto unknown compounds bearing the oxydiazene oxide and oxytriazene oxide units bridged by the methylene group via the oxygen atoms. The synthesized compounds are of interest as potential nitric oxide donors in living organisms. Smirnov, G. A. aut Enthalten in Russian chemical bulletin New York, NY [u.a.] : Consultants Bureau, 1952 72(2023), 7 vom: Juli, Seite 1584-1590 (DE-627)325573417 (DE-600)2037677-7 1573-9171 nnns volume:72 year:2023 number:7 month:07 pages:1584-1590 https://dx.doi.org/10.1007/s11172-023-3937-4 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_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 72 2023 7 07 1584-1590
allfieldsSound	10.1007/s11172-023-3937-4 doi (DE-627)SPR052616967 (SPR)s11172-023-3937-4-e DE-627 ger DE-627 rakwb eng Gordeev, P. B. verfasserin aut Alkylation of oxytriazene oxide salts with 2-(chloromethoxy)diazene 1-oxide derivatives 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer Science+Business Media LLC 2023 Abstract A general synthesis of 2-chloromethoxy-1-diazene oxides from their salts was developed. Alkylation of the sodium salts of oxytriazene oxides with 2-chloromethoxy-1-diazene oxides gave hitherto unknown compounds bearing the oxydiazene oxide and oxytriazene oxide units bridged by the methylene group via the oxygen atoms. The synthesized compounds are of interest as potential nitric oxide donors in living organisms. Smirnov, G. A. aut Enthalten in Russian chemical bulletin New York, NY [u.a.] : Consultants Bureau, 1952 72(2023), 7 vom: Juli, Seite 1584-1590 (DE-627)325573417 (DE-600)2037677-7 1573-9171 nnns volume:72 year:2023 number:7 month:07 pages:1584-1590 https://dx.doi.org/10.1007/s11172-023-3937-4 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_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 72 2023 7 07 1584-1590
language	English
source	Enthalten in Russian chemical bulletin 72(2023), 7 vom: Juli, Seite 1584-1590 volume:72 year:2023 number:7 month:07 pages:1584-1590
sourceStr	Enthalten in Russian chemical bulletin 72(2023), 7 vom: Juli, Seite 1584-1590 volume:72 year:2023 number:7 month:07 pages:1584-1590
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container_title	Russian chemical bulletin
authorswithroles_txt_mv	Gordeev, P. B. @@aut@@ Smirnov, G. A. @@aut@@
publishDateDaySort_date	2023-07-01T00:00:00Z
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id	SPR052616967
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author	Gordeev, P. B.
spellingShingle	Gordeev, P. B. Alkylation of oxytriazene oxide salts with 2-(chloromethoxy)diazene 1-oxide derivatives
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topic_title	Alkylation of oxytriazene oxide salts with 2-(chloromethoxy)diazene 1-oxide derivatives
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title	Alkylation of oxytriazene oxide salts with 2-(chloromethoxy)diazene 1-oxide derivatives
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title_full	Alkylation of oxytriazene oxide salts with 2-(chloromethoxy)diazene 1-oxide derivatives
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doi_str_mv	10.1007/s11172-023-3937-4
title_sort	alkylation of oxytriazene oxide salts with 2-(chloromethoxy)diazene 1-oxide derivatives
title_auth	Alkylation of oxytriazene oxide salts with 2-(chloromethoxy)diazene 1-oxide derivatives
abstract	Abstract A general synthesis of 2-chloromethoxy-1-diazene oxides from their salts was developed. Alkylation of the sodium salts of oxytriazene oxides with 2-chloromethoxy-1-diazene oxides gave hitherto unknown compounds bearing the oxydiazene oxide and oxytriazene oxide units bridged by the methylene group via the oxygen atoms. The synthesized compounds are of interest as potential nitric oxide donors in living organisms. © Springer Science+Business Media LLC 2023
abstractGer	Abstract A general synthesis of 2-chloromethoxy-1-diazene oxides from their salts was developed. Alkylation of the sodium salts of oxytriazene oxides with 2-chloromethoxy-1-diazene oxides gave hitherto unknown compounds bearing the oxydiazene oxide and oxytriazene oxide units bridged by the methylene group via the oxygen atoms. The synthesized compounds are of interest as potential nitric oxide donors in living organisms. © Springer Science+Business Media LLC 2023
abstract_unstemmed	Abstract A general synthesis of 2-chloromethoxy-1-diazene oxides from their salts was developed. Alkylation of the sodium salts of oxytriazene oxides with 2-chloromethoxy-1-diazene oxides gave hitherto unknown compounds bearing the oxydiazene oxide and oxytriazene oxide units bridged by the methylene group via the oxygen atoms. The synthesized compounds are of interest as potential nitric oxide donors in living organisms. © Springer Science+Business Media LLC 2023
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title_short	Alkylation of oxytriazene oxide salts with 2-(chloromethoxy)diazene 1-oxide derivatives
url	https://dx.doi.org/10.1007/s11172-023-3937-4
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Alkylation of the sodium salts of oxytriazene oxides with 2-chloromethoxy-1-diazene oxides gave hitherto unknown compounds bearing the oxydiazene oxide and oxytriazene oxide units bridged by the methylene group via the oxygen atoms. The synthesized compounds are of interest as potential nitric oxide donors in living organisms.</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Smirnov, G. 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Alkylation of oxytriazene oxide salts with 2-(chloromethoxy)diazene 1-oxide derivatives

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