Transformation of triterpene ketoximes into lactams by the action of ozone
The principal ozonoysis products of triterpene ketoximes and O-methylketoximes in $ CH_{2} %$ Cl_{2} $ at 0°C were triterpene lactams and N-methoxylactams.
Gespeichert in:
| Autor*in: |
Kazakova, O. B. [verfasserIn] Yamansarov, E. Yu. [verfasserIn] Kukovinets, O. S. [verfasserIn] Medvedeva, N. I. [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2011 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Chemistry of natural compounds - New York, NY [u.a.] : Consultants Bureau, 1965, 47(2011), 5 vom: Nov., Seite 749-751 |
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| Übergeordnetes Werk: |
volume:47 ; year:2011 ; number:5 ; month:11 ; pages:749-751 |
| Links: |
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| DOI / URN: |
10.1007/s10600-011-0049-4 |
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| Katalog-ID: |
SPR011819936 |
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| 520 | |a The principal ozonoysis products of triterpene ketoximes and O-methylketoximes in $ CH_{2} %$ Cl_{2} $ at 0°C were triterpene lactams and N-methoxylactams. | ||
| 650 | 4 | |a triterpenoids |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a ozone |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a ketoximes |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a lactams |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Yamansarov, E. Yu. |e verfasserin |4 aut | |
| 700 | 1 | |a Kukovinets, O. S. |e verfasserin |4 aut | |
| 700 | 1 | |a Medvedeva, N. I. |e verfasserin |4 aut | |
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10.1007/s10600-011-0049-4 doi (DE-627)SPR011819936 (SPR)s10600-011-0049-4-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Kazakova, O. B. verfasserin aut Transformation of triterpene ketoximes into lactams by the action of ozone 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The principal ozonoysis products of triterpene ketoximes and O-methylketoximes in $ CH_{2} %$ Cl_{2} $ at 0°C were triterpene lactams and N-methoxylactams. triterpenoids (dpeaa)DE-He213 ozone (dpeaa)DE-He213 ketoximes (dpeaa)DE-He213 lactams (dpeaa)DE-He213 Yamansarov, E. Yu. verfasserin aut Kukovinets, O. S. verfasserin aut Medvedeva, N. I. verfasserin aut Enthalten in Chemistry of natural compounds New York, NY [u.a.] : Consultants Bureau, 1965 47(2011), 5 vom: Nov., Seite 749-751 (DE-627)325568618 (DE-600)2037133-0 1573-8388 nnns volume:47 year:2011 number:5 month:11 pages:749-751 https://dx.doi.org/10.1007/s10600-011-0049-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_2070 GBV_ILN_2086 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_2116 GBV_ILN_2118 GBV_ILN_2119 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_4012 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 ASE AR 47 2011 5 11 749-751 |
| spelling |
10.1007/s10600-011-0049-4 doi (DE-627)SPR011819936 (SPR)s10600-011-0049-4-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Kazakova, O. B. verfasserin aut Transformation of triterpene ketoximes into lactams by the action of ozone 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The principal ozonoysis products of triterpene ketoximes and O-methylketoximes in $ CH_{2} %$ Cl_{2} $ at 0°C were triterpene lactams and N-methoxylactams. triterpenoids (dpeaa)DE-He213 ozone (dpeaa)DE-He213 ketoximes (dpeaa)DE-He213 lactams (dpeaa)DE-He213 Yamansarov, E. Yu. verfasserin aut Kukovinets, O. S. verfasserin aut Medvedeva, N. I. verfasserin aut Enthalten in Chemistry of natural compounds New York, NY [u.a.] : Consultants Bureau, 1965 47(2011), 5 vom: Nov., Seite 749-751 (DE-627)325568618 (DE-600)2037133-0 1573-8388 nnns volume:47 year:2011 number:5 month:11 pages:749-751 https://dx.doi.org/10.1007/s10600-011-0049-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_2070 GBV_ILN_2086 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_2116 GBV_ILN_2118 GBV_ILN_2119 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_4012 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 ASE AR 47 2011 5 11 749-751 |
| allfields_unstemmed |
10.1007/s10600-011-0049-4 doi (DE-627)SPR011819936 (SPR)s10600-011-0049-4-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Kazakova, O. B. verfasserin aut Transformation of triterpene ketoximes into lactams by the action of ozone 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The principal ozonoysis products of triterpene ketoximes and O-methylketoximes in $ CH_{2} %$ Cl_{2} $ at 0°C were triterpene lactams and N-methoxylactams. triterpenoids (dpeaa)DE-He213 ozone (dpeaa)DE-He213 ketoximes (dpeaa)DE-He213 lactams (dpeaa)DE-He213 Yamansarov, E. Yu. verfasserin aut Kukovinets, O. S. verfasserin aut Medvedeva, N. I. verfasserin aut Enthalten in Chemistry of natural compounds New York, NY [u.a.] : Consultants Bureau, 1965 47(2011), 5 vom: Nov., Seite 749-751 (DE-627)325568618 (DE-600)2037133-0 1573-8388 nnns volume:47 year:2011 number:5 month:11 pages:749-751 https://dx.doi.org/10.1007/s10600-011-0049-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_2070 GBV_ILN_2086 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_2116 GBV_ILN_2118 GBV_ILN_2119 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_4012 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 ASE AR 47 2011 5 11 749-751 |
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10.1007/s10600-011-0049-4 doi (DE-627)SPR011819936 (SPR)s10600-011-0049-4-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Kazakova, O. B. verfasserin aut Transformation of triterpene ketoximes into lactams by the action of ozone 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The principal ozonoysis products of triterpene ketoximes and O-methylketoximes in $ CH_{2} %$ Cl_{2} $ at 0°C were triterpene lactams and N-methoxylactams. triterpenoids (dpeaa)DE-He213 ozone (dpeaa)DE-He213 ketoximes (dpeaa)DE-He213 lactams (dpeaa)DE-He213 Yamansarov, E. Yu. verfasserin aut Kukovinets, O. S. verfasserin aut Medvedeva, N. I. verfasserin aut Enthalten in Chemistry of natural compounds New York, NY [u.a.] : Consultants Bureau, 1965 47(2011), 5 vom: Nov., Seite 749-751 (DE-627)325568618 (DE-600)2037133-0 1573-8388 nnns volume:47 year:2011 number:5 month:11 pages:749-751 https://dx.doi.org/10.1007/s10600-011-0049-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_2070 GBV_ILN_2086 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_2116 GBV_ILN_2118 GBV_ILN_2119 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_4012 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 ASE AR 47 2011 5 11 749-751 |
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10.1007/s10600-011-0049-4 doi (DE-627)SPR011819936 (SPR)s10600-011-0049-4-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Kazakova, O. B. verfasserin aut Transformation of triterpene ketoximes into lactams by the action of ozone 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier The principal ozonoysis products of triterpene ketoximes and O-methylketoximes in $ CH_{2} %$ Cl_{2} $ at 0°C were triterpene lactams and N-methoxylactams. triterpenoids (dpeaa)DE-He213 ozone (dpeaa)DE-He213 ketoximes (dpeaa)DE-He213 lactams (dpeaa)DE-He213 Yamansarov, E. Yu. verfasserin aut Kukovinets, O. S. verfasserin aut Medvedeva, N. I. verfasserin aut Enthalten in Chemistry of natural compounds New York, NY [u.a.] : Consultants Bureau, 1965 47(2011), 5 vom: Nov., Seite 749-751 (DE-627)325568618 (DE-600)2037133-0 1573-8388 nnns volume:47 year:2011 number:5 month:11 pages:749-751 https://dx.doi.org/10.1007/s10600-011-0049-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_2070 GBV_ILN_2086 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_2116 GBV_ILN_2118 GBV_ILN_2119 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_4012 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_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 35.00 ASE AR 47 2011 5 11 749-751 |
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English |
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Enthalten in Chemistry of natural compounds 47(2011), 5 vom: Nov., Seite 749-751 volume:47 year:2011 number:5 month:11 pages:749-751 |
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Enthalten in Chemistry of natural compounds 47(2011), 5 vom: Nov., Seite 749-751 volume:47 year:2011 number:5 month:11 pages:749-751 |
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Article |
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findex.gbv.de |
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triterpenoids ozone ketoximes lactams |
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540 |
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| container_title |
Chemistry of natural compounds |
| authorswithroles_txt_mv |
Kazakova, O. B. @@aut@@ Yamansarov, E. Yu. @@aut@@ Kukovinets, O. S. @@aut@@ Medvedeva, N. I. @@aut@@ |
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2011-11-01T00:00:00Z |
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325568618 |
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3540 |
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SPR011819936 |
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englisch |
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Kazakova, O. B. |
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Kazakova, O. B. ddc 540 bkl 35.00 misc triterpenoids misc ozone misc ketoximes misc lactams Transformation of triterpene ketoximes into lactams by the action of ozone |
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540 ASE 35.00 bkl Transformation of triterpene ketoximes into lactams by the action of ozone triterpenoids (dpeaa)DE-He213 ozone (dpeaa)DE-He213 ketoximes (dpeaa)DE-He213 lactams (dpeaa)DE-He213 |
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Transformation of triterpene ketoximes into lactams by the action of ozone |
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Transformation of triterpene ketoximes into lactams by the action of ozone |
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Kazakova, O. B. |
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Kazakova, O. B. Yamansarov, E. Yu. Kukovinets, O. S. Medvedeva, N. I. |
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transformation of triterpene ketoximes into lactams by the action of ozone |
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Transformation of triterpene ketoximes into lactams by the action of ozone |
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The principal ozonoysis products of triterpene ketoximes and O-methylketoximes in $ CH_{2} %$ Cl_{2} $ at 0°C were triterpene lactams and N-methoxylactams. |
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The principal ozonoysis products of triterpene ketoximes and O-methylketoximes in $ CH_{2} %$ Cl_{2} $ at 0°C were triterpene lactams and N-methoxylactams. |
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The principal ozonoysis products of triterpene ketoximes and O-methylketoximes in $ CH_{2} %$ Cl_{2} $ at 0°C were triterpene lactams and N-methoxylactams. |
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Transformation of triterpene ketoximes into lactams by the action of ozone |
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