Structure of fumaridine and fumaramine
Conclusions The most probable structures have been proposed for fumaridine and fumaramine on the basis of their spectral characteristics and chemical transformations.
Gespeichert in:
| Autor*in: |
Israilov, I. A. [verfasserIn] Yunusov, M. S. [verfasserIn] Yunusov, S. Yu. [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
1970 |
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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, 6(1970), 5 vom: 01. Sept., Seite 603-605 |
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| Übergeordnetes Werk: |
volume:6 ; year:1970 ; number:5 ; day:01 ; month:09 ; pages:603-605 |
| Links: |
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| DOI / URN: |
10.1007/BF00563451 |
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| Katalog-ID: |
SPR011691336 |
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| 100 | 1 | |a Israilov, I. A. |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Structure of fumaridine and fumaramine |
| 264 | 1 | |c 1970 | |
| 336 | |a Text |b txt |2 rdacontent | ||
| 337 | |a Computermedien |b c |2 rdamedia | ||
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| 520 | |a Conclusions The most probable structures have been proposed for fumaridine and fumaramine on the basis of their spectral characteristics and chemical transformations. | ||
| 650 | 4 | |a Hydrobromide |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Olefinic Proton |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Methiodide |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Deuterochloroform |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Platinum Black |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Yunusov, M. S. |e verfasserin |4 aut | |
| 700 | 1 | |a Yunusov, S. Yu. |e verfasserin |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t Chemistry of natural compounds |d New York, NY [u.a.] : Consultants Bureau, 1965 |g 6(1970), 5 vom: 01. Sept., Seite 603-605 |w (DE-627)325568618 |w (DE-600)2037133-0 |x 1573-8388 |7 nnns |
| 773 | 1 | 8 | |g volume:6 |g year:1970 |g number:5 |g day:01 |g month:09 |g pages:603-605 |
| 856 | 4 | 0 | |u https://dx.doi.org/10.1007/BF00563451 |z lizenzpflichtig |3 Volltext |
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| 912 | |a GBV_ILN_121 | ||
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| 912 | |a GBV_ILN_2004 | ||
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| 912 | |a GBV_ILN_2020 | ||
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| 912 | |a GBV_ILN_2034 | ||
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| 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_2116 | ||
| 912 | |a GBV_ILN_2118 | ||
| 912 | |a GBV_ILN_2119 | ||
| 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_2158 | ||
| 912 | |a GBV_ILN_2188 | ||
| 912 | |a GBV_ILN_2190 | ||
| 912 | |a GBV_ILN_2193 | ||
| 912 | |a GBV_ILN_2232 | ||
| 912 | |a GBV_ILN_2336 | ||
| 912 | |a GBV_ILN_2446 | ||
| 912 | |a GBV_ILN_2470 | ||
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| 912 | |a GBV_ILN_4251 | ||
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| 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 | ||
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| 936 | b | k | |a 35.00 |q ASE |
| 951 | |a AR | ||
| 952 | |d 6 |j 1970 |e 5 |b 01 |c 09 |h 603-605 | ||
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| hierarchy_sort_str |
1970 |
| bklnumber |
35.00 |
| publishDate |
1970 |
| allfields |
10.1007/BF00563451 doi (DE-627)SPR011691336 (SPR)BF00563451-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Israilov, I. A. verfasserin aut Structure of fumaridine and fumaramine 1970 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Conclusions The most probable structures have been proposed for fumaridine and fumaramine on the basis of their spectral characteristics and chemical transformations. Hydrobromide (dpeaa)DE-He213 Olefinic Proton (dpeaa)DE-He213 Methiodide (dpeaa)DE-He213 Deuterochloroform (dpeaa)DE-He213 Platinum Black (dpeaa)DE-He213 Yunusov, M. S. verfasserin aut Yunusov, S. Yu. verfasserin aut Enthalten in Chemistry of natural compounds New York, NY [u.a.] : Consultants Bureau, 1965 6(1970), 5 vom: 01. Sept., Seite 603-605 (DE-627)325568618 (DE-600)2037133-0 1573-8388 nnns volume:6 year:1970 number:5 day:01 month:09 pages:603-605 https://dx.doi.org/10.1007/BF00563451 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_121 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_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_647 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_2018 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_2043 GBV_ILN_2044 GBV_ILN_2048 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_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_2158 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2193 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_2808 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_4277 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_4346 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 GBV_ILN_4753 35.00 ASE AR 6 1970 5 01 09 603-605 |
| spelling |
10.1007/BF00563451 doi (DE-627)SPR011691336 (SPR)BF00563451-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Israilov, I. A. verfasserin aut Structure of fumaridine and fumaramine 1970 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Conclusions The most probable structures have been proposed for fumaridine and fumaramine on the basis of their spectral characteristics and chemical transformations. Hydrobromide (dpeaa)DE-He213 Olefinic Proton (dpeaa)DE-He213 Methiodide (dpeaa)DE-He213 Deuterochloroform (dpeaa)DE-He213 Platinum Black (dpeaa)DE-He213 Yunusov, M. S. verfasserin aut Yunusov, S. Yu. verfasserin aut Enthalten in Chemistry of natural compounds New York, NY [u.a.] : Consultants Bureau, 1965 6(1970), 5 vom: 01. Sept., Seite 603-605 (DE-627)325568618 (DE-600)2037133-0 1573-8388 nnns volume:6 year:1970 number:5 day:01 month:09 pages:603-605 https://dx.doi.org/10.1007/BF00563451 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_121 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_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_647 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_2018 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_2043 GBV_ILN_2044 GBV_ILN_2048 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_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_2158 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2193 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_2808 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_4277 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_4346 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 GBV_ILN_4753 35.00 ASE AR 6 1970 5 01 09 603-605 |
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10.1007/BF00563451 doi (DE-627)SPR011691336 (SPR)BF00563451-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Israilov, I. A. verfasserin aut Structure of fumaridine and fumaramine 1970 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Conclusions The most probable structures have been proposed for fumaridine and fumaramine on the basis of their spectral characteristics and chemical transformations. Hydrobromide (dpeaa)DE-He213 Olefinic Proton (dpeaa)DE-He213 Methiodide (dpeaa)DE-He213 Deuterochloroform (dpeaa)DE-He213 Platinum Black (dpeaa)DE-He213 Yunusov, M. S. verfasserin aut Yunusov, S. Yu. verfasserin aut Enthalten in Chemistry of natural compounds New York, NY [u.a.] : Consultants Bureau, 1965 6(1970), 5 vom: 01. Sept., Seite 603-605 (DE-627)325568618 (DE-600)2037133-0 1573-8388 nnns volume:6 year:1970 number:5 day:01 month:09 pages:603-605 https://dx.doi.org/10.1007/BF00563451 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_121 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_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_647 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_2018 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_2043 GBV_ILN_2044 GBV_ILN_2048 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_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_2158 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2193 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_2808 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_4277 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_4346 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 GBV_ILN_4753 35.00 ASE AR 6 1970 5 01 09 603-605 |
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10.1007/BF00563451 doi (DE-627)SPR011691336 (SPR)BF00563451-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Israilov, I. A. verfasserin aut Structure of fumaridine and fumaramine 1970 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Conclusions The most probable structures have been proposed for fumaridine and fumaramine on the basis of their spectral characteristics and chemical transformations. Hydrobromide (dpeaa)DE-He213 Olefinic Proton (dpeaa)DE-He213 Methiodide (dpeaa)DE-He213 Deuterochloroform (dpeaa)DE-He213 Platinum Black (dpeaa)DE-He213 Yunusov, M. S. verfasserin aut Yunusov, S. Yu. verfasserin aut Enthalten in Chemistry of natural compounds New York, NY [u.a.] : Consultants Bureau, 1965 6(1970), 5 vom: 01. Sept., Seite 603-605 (DE-627)325568618 (DE-600)2037133-0 1573-8388 nnns volume:6 year:1970 number:5 day:01 month:09 pages:603-605 https://dx.doi.org/10.1007/BF00563451 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_121 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_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_647 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_2018 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_2043 GBV_ILN_2044 GBV_ILN_2048 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_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_2158 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2193 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_2808 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_4277 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_4346 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 GBV_ILN_4753 35.00 ASE AR 6 1970 5 01 09 603-605 |
| allfieldsSound |
10.1007/BF00563451 doi (DE-627)SPR011691336 (SPR)BF00563451-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Israilov, I. A. verfasserin aut Structure of fumaridine and fumaramine 1970 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Conclusions The most probable structures have been proposed for fumaridine and fumaramine on the basis of their spectral characteristics and chemical transformations. Hydrobromide (dpeaa)DE-He213 Olefinic Proton (dpeaa)DE-He213 Methiodide (dpeaa)DE-He213 Deuterochloroform (dpeaa)DE-He213 Platinum Black (dpeaa)DE-He213 Yunusov, M. S. verfasserin aut Yunusov, S. Yu. verfasserin aut Enthalten in Chemistry of natural compounds New York, NY [u.a.] : Consultants Bureau, 1965 6(1970), 5 vom: 01. Sept., Seite 603-605 (DE-627)325568618 (DE-600)2037133-0 1573-8388 nnns volume:6 year:1970 number:5 day:01 month:09 pages:603-605 https://dx.doi.org/10.1007/BF00563451 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_121 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_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_647 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_2018 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_2043 GBV_ILN_2044 GBV_ILN_2048 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_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_2158 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2193 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_2808 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_4277 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_4346 GBV_ILN_4367 GBV_ILN_4393 GBV_ILN_4700 GBV_ILN_4753 35.00 ASE AR 6 1970 5 01 09 603-605 |
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English |
| source |
Enthalten in Chemistry of natural compounds 6(1970), 5 vom: 01. Sept., Seite 603-605 volume:6 year:1970 number:5 day:01 month:09 pages:603-605 |
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Enthalten in Chemistry of natural compounds 6(1970), 5 vom: 01. Sept., Seite 603-605 volume:6 year:1970 number:5 day:01 month:09 pages:603-605 |
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findex.gbv.de |
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Hydrobromide Olefinic Proton Methiodide Deuterochloroform Platinum Black |
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false |
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Chemistry of natural compounds |
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Israilov, I. A. @@aut@@ Yunusov, M. S. @@aut@@ Yunusov, S. Yu. @@aut@@ |
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1970-09-01T00:00:00Z |
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3540 |
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Israilov, I. A. |
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Israilov, I. A. ddc 540 bkl 35.00 misc Hydrobromide misc Olefinic Proton misc Methiodide misc Deuterochloroform misc Platinum Black Structure of fumaridine and fumaramine |
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540 ASE 35.00 bkl Structure of fumaridine and fumaramine Hydrobromide (dpeaa)DE-He213 Olefinic Proton (dpeaa)DE-He213 Methiodide (dpeaa)DE-He213 Deuterochloroform (dpeaa)DE-He213 Platinum Black (dpeaa)DE-He213 |
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ddc 540 bkl 35.00 misc Hydrobromide misc Olefinic Proton misc Methiodide misc Deuterochloroform misc Platinum Black |
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ddc 540 bkl 35.00 misc Hydrobromide misc Olefinic Proton misc Methiodide misc Deuterochloroform misc Platinum Black |
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ddc 540 bkl 35.00 misc Hydrobromide misc Olefinic Proton misc Methiodide misc Deuterochloroform misc Platinum Black |
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Structure of fumaridine and fumaramine |
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Structure of fumaridine and fumaramine |
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Israilov, I. A. |
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Chemistry of natural compounds |
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Israilov, I. A. Yunusov, M. S. Yunusov, S. Yu. |
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structure of fumaridine and fumaramine |
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Structure of fumaridine and fumaramine |
| abstract |
Conclusions The most probable structures have been proposed for fumaridine and fumaramine on the basis of their spectral characteristics and chemical transformations. |
| abstractGer |
Conclusions The most probable structures have been proposed for fumaridine and fumaramine on the basis of their spectral characteristics and chemical transformations. |
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Conclusions The most probable structures have been proposed for fumaridine and fumaramine on the basis of their spectral characteristics and chemical transformations. |
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Structure of fumaridine and fumaramine |
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2024-07-04T00:00:36.762Z |
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