Structure and absolute configuration of collutine

Summary A new base with the composition $ C_{21} %$ H_{25} %$ O_{5} $N, mp 192–194°C, [α]D -182°C, which has been called collutine, has been isolated from the epigeal parts ofColchicum luteum Baker. On the basis of UV, IR, NMR, and mass spectra and chemical reactions, the structure of 4-hydroxy-2,3,...
Ausführliche Beschreibung

Gespeichert in:

Autor*in:	Mukhamed'yarova, N. L. [verfasserIn] Yusupov, M. K. [verfasserIn] Aslanov, Kh. A. [verfasserIn] Sadykov, A. S. [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	1975

Schlagwörter:	Alkaloid Absolute Configuration Epigeal Part Methiodide Tropolone

Übergeordnetes Werk:	Enthalten in: Chemistry of natural compounds - New York, NY [u.a.] : Consultants Bureau, 1965, 11(1975), 6 vom: 01. Nov., Seite 781-783
Übergeordnetes Werk:	volume:11 ; year:1975 ; number:6 ; day:01 ; month:11 ; pages:781-783

Links:	Volltext

DOI / URN:	10.1007/BF00568470

Katalog-ID:	SPR011704713

Internformat


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520			\|a Summary A new base with the composition $ C_{21} %$ H_{25} %$ O_{5} $N, mp 192–194°C, [α]D -182°C, which has been called collutine, has been isolated from the epigeal parts ofColchicum luteum Baker. On the basis of UV, IR, NMR, and mass spectra and chemical reactions, the structure of 4-hydroxy-2,3, 6-trimethoxyhomomorphinandienone has been proposed for collutine.
650		4	\|a Alkaloid \|7 (dpeaa)DE-He213
650		4	\|a Absolute Configuration \|7 (dpeaa)DE-He213
650		4	\|a Epigeal Part \|7 (dpeaa)DE-He213
650		4	\|a Methiodide \|7 (dpeaa)DE-He213
650		4	\|a Tropolone \|7 (dpeaa)DE-He213
700	1		\|a Yusupov, M. K. \|e verfasserin \|4 aut
700	1		\|a Aslanov, Kh. A. \|e verfasserin \|4 aut
700	1		\|a Sadykov, A. S. \|e verfasserin \|4 aut
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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_121
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_285
912			\|a GBV_ILN_293
912			\|a GBV_ILN_370
912			\|a GBV_ILN_374
912			\|a GBV_ILN_602
912			\|a GBV_ILN_647
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_2018
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_2043
912			\|a GBV_ILN_2044
912			\|a GBV_ILN_2048
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_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
912			\|a GBV_ILN_2472
912			\|a GBV_ILN_2507
912			\|a GBV_ILN_2522
912			\|a GBV_ILN_2548
912			\|a GBV_ILN_2808
912			\|a GBV_ILN_4012
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_4277
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_4346
912			\|a GBV_ILN_4367
912			\|a GBV_ILN_4393
912			\|a GBV_ILN_4700
912			\|a GBV_ILN_4753
936	b	k	\|a 35.00 \|q ASE
951			\|a AR
952			\|d 11 \|j 1975 \|e 6 \|b 01 \|c 11 \|h 781-783

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publishDate	1975
allfields	10.1007/BF00568470 doi (DE-627)SPR011704713 (SPR)BF00568470-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Mukhamed'yarova, N. L. verfasserin aut Structure and absolute configuration of collutine 1975 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Summary A new base with the composition $ C_{21} %$ H_{25} %$ O_{5} $N, mp 192–194°C, [α]D -182°C, which has been called collutine, has been isolated from the epigeal parts ofColchicum luteum Baker. On the basis of UV, IR, NMR, and mass spectra and chemical reactions, the structure of 4-hydroxy-2,3, 6-trimethoxyhomomorphinandienone has been proposed for collutine. Alkaloid (dpeaa)DE-He213 Absolute Configuration (dpeaa)DE-He213 Epigeal Part (dpeaa)DE-He213 Methiodide (dpeaa)DE-He213 Tropolone (dpeaa)DE-He213 Yusupov, M. K. verfasserin aut Aslanov, Kh. A. verfasserin aut Sadykov, A. S. verfasserin aut Enthalten in Chemistry of natural compounds New York, NY [u.a.] : Consultants Bureau, 1965 11(1975), 6 vom: 01. Nov., Seite 781-783 (DE-627)325568618 (DE-600)2037133-0 1573-8388 nnns volume:11 year:1975 number:6 day:01 month:11 pages:781-783 https://dx.doi.org/10.1007/BF00568470 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 11 1975 6 01 11 781-783
spelling	10.1007/BF00568470 doi (DE-627)SPR011704713 (SPR)BF00568470-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Mukhamed'yarova, N. L. verfasserin aut Structure and absolute configuration of collutine 1975 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Summary A new base with the composition $ C_{21} %$ H_{25} %$ O_{5} $N, mp 192–194°C, [α]D -182°C, which has been called collutine, has been isolated from the epigeal parts ofColchicum luteum Baker. On the basis of UV, IR, NMR, and mass spectra and chemical reactions, the structure of 4-hydroxy-2,3, 6-trimethoxyhomomorphinandienone has been proposed for collutine. Alkaloid (dpeaa)DE-He213 Absolute Configuration (dpeaa)DE-He213 Epigeal Part (dpeaa)DE-He213 Methiodide (dpeaa)DE-He213 Tropolone (dpeaa)DE-He213 Yusupov, M. K. verfasserin aut Aslanov, Kh. A. verfasserin aut Sadykov, A. S. verfasserin aut Enthalten in Chemistry of natural compounds New York, NY [u.a.] : Consultants Bureau, 1965 11(1975), 6 vom: 01. Nov., Seite 781-783 (DE-627)325568618 (DE-600)2037133-0 1573-8388 nnns volume:11 year:1975 number:6 day:01 month:11 pages:781-783 https://dx.doi.org/10.1007/BF00568470 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 11 1975 6 01 11 781-783
allfields_unstemmed	10.1007/BF00568470 doi (DE-627)SPR011704713 (SPR)BF00568470-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Mukhamed'yarova, N. L. verfasserin aut Structure and absolute configuration of collutine 1975 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Summary A new base with the composition $ C_{21} %$ H_{25} %$ O_{5} $N, mp 192–194°C, [α]D -182°C, which has been called collutine, has been isolated from the epigeal parts ofColchicum luteum Baker. On the basis of UV, IR, NMR, and mass spectra and chemical reactions, the structure of 4-hydroxy-2,3, 6-trimethoxyhomomorphinandienone has been proposed for collutine. Alkaloid (dpeaa)DE-He213 Absolute Configuration (dpeaa)DE-He213 Epigeal Part (dpeaa)DE-He213 Methiodide (dpeaa)DE-He213 Tropolone (dpeaa)DE-He213 Yusupov, M. K. verfasserin aut Aslanov, Kh. A. verfasserin aut Sadykov, A. S. verfasserin aut Enthalten in Chemistry of natural compounds New York, NY [u.a.] : Consultants Bureau, 1965 11(1975), 6 vom: 01. Nov., Seite 781-783 (DE-627)325568618 (DE-600)2037133-0 1573-8388 nnns volume:11 year:1975 number:6 day:01 month:11 pages:781-783 https://dx.doi.org/10.1007/BF00568470 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 11 1975 6 01 11 781-783
allfieldsGer	10.1007/BF00568470 doi (DE-627)SPR011704713 (SPR)BF00568470-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Mukhamed'yarova, N. L. verfasserin aut Structure and absolute configuration of collutine 1975 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Summary A new base with the composition $ C_{21} %$ H_{25} %$ O_{5} $N, mp 192–194°C, [α]D -182°C, which has been called collutine, has been isolated from the epigeal parts ofColchicum luteum Baker. On the basis of UV, IR, NMR, and mass spectra and chemical reactions, the structure of 4-hydroxy-2,3, 6-trimethoxyhomomorphinandienone has been proposed for collutine. Alkaloid (dpeaa)DE-He213 Absolute Configuration (dpeaa)DE-He213 Epigeal Part (dpeaa)DE-He213 Methiodide (dpeaa)DE-He213 Tropolone (dpeaa)DE-He213 Yusupov, M. K. verfasserin aut Aslanov, Kh. A. verfasserin aut Sadykov, A. S. verfasserin aut Enthalten in Chemistry of natural compounds New York, NY [u.a.] : Consultants Bureau, 1965 11(1975), 6 vom: 01. Nov., Seite 781-783 (DE-627)325568618 (DE-600)2037133-0 1573-8388 nnns volume:11 year:1975 number:6 day:01 month:11 pages:781-783 https://dx.doi.org/10.1007/BF00568470 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 11 1975 6 01 11 781-783
allfieldsSound	10.1007/BF00568470 doi (DE-627)SPR011704713 (SPR)BF00568470-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Mukhamed'yarova, N. L. verfasserin aut Structure and absolute configuration of collutine 1975 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Summary A new base with the composition $ C_{21} %$ H_{25} %$ O_{5} $N, mp 192–194°C, [α]D -182°C, which has been called collutine, has been isolated from the epigeal parts ofColchicum luteum Baker. On the basis of UV, IR, NMR, and mass spectra and chemical reactions, the structure of 4-hydroxy-2,3, 6-trimethoxyhomomorphinandienone has been proposed for collutine. Alkaloid (dpeaa)DE-He213 Absolute Configuration (dpeaa)DE-He213 Epigeal Part (dpeaa)DE-He213 Methiodide (dpeaa)DE-He213 Tropolone (dpeaa)DE-He213 Yusupov, M. K. verfasserin aut Aslanov, Kh. A. verfasserin aut Sadykov, A. S. verfasserin aut Enthalten in Chemistry of natural compounds New York, NY [u.a.] : Consultants Bureau, 1965 11(1975), 6 vom: 01. Nov., Seite 781-783 (DE-627)325568618 (DE-600)2037133-0 1573-8388 nnns volume:11 year:1975 number:6 day:01 month:11 pages:781-783 https://dx.doi.org/10.1007/BF00568470 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 11 1975 6 01 11 781-783
language	English
source	Enthalten in Chemistry of natural compounds 11(1975), 6 vom: 01. Nov., Seite 781-783 volume:11 year:1975 number:6 day:01 month:11 pages:781-783
sourceStr	Enthalten in Chemistry of natural compounds 11(1975), 6 vom: 01. Nov., Seite 781-783 volume:11 year:1975 number:6 day:01 month:11 pages:781-783
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	Alkaloid Absolute Configuration Epigeal Part Methiodide Tropolone
dewey-raw	540
isfreeaccess_bool	false
container_title	Chemistry of natural compounds
authorswithroles_txt_mv	Mukhamed'yarova, N. L. @@aut@@ Yusupov, M. K. @@aut@@ Aslanov, Kh. A. @@aut@@ Sadykov, A. S. @@aut@@
publishDateDaySort_date	1975-11-01T00:00:00Z
hierarchy_top_id	325568618
dewey-sort	3540
id	SPR011704713
language_de	englisch
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L.</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Structure and absolute configuration of collutine</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">1975</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Summary A new base with the composition $ C_{21} %$ H_{25} %$ O_{5} $N, mp 192–194°C, [α]D -182°C, which has been called collutine, has been isolated from the epigeal parts ofColchicum luteum Baker. 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author	Mukhamed'yarova, N. L.
spellingShingle	Mukhamed'yarova, N. L. ddc 540 bkl 35.00 misc Alkaloid misc Absolute Configuration misc Epigeal Part misc Methiodide misc Tropolone Structure and absolute configuration of collutine
authorStr	Mukhamed'yarova, N. L.
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topic_title	540 ASE 35.00 bkl Structure and absolute configuration of collutine Alkaloid (dpeaa)DE-He213 Absolute Configuration (dpeaa)DE-He213 Epigeal Part (dpeaa)DE-He213 Methiodide (dpeaa)DE-He213 Tropolone (dpeaa)DE-He213
topic	ddc 540 bkl 35.00 misc Alkaloid misc Absolute Configuration misc Epigeal Part misc Methiodide misc Tropolone
topic_unstemmed	ddc 540 bkl 35.00 misc Alkaloid misc Absolute Configuration misc Epigeal Part misc Methiodide misc Tropolone
topic_browse	ddc 540 bkl 35.00 misc Alkaloid misc Absolute Configuration misc Epigeal Part misc Methiodide misc Tropolone
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title	Structure and absolute configuration of collutine
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title_full	Structure and absolute configuration of collutine
author_sort	Mukhamed'yarova, N. L.
journal	Chemistry of natural compounds
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author_browse	Mukhamed'yarova, N. L. Yusupov, M. K. Aslanov, Kh. A. Sadykov, A. S.
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author-letter	Mukhamed'yarova, N. L.
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title_sort	structure and absolute configuration of collutine
title_auth	Structure and absolute configuration of collutine
abstract	Summary A new base with the composition $ C_{21} %$ H_{25} %$ O_{5} $N, mp 192–194°C, [α]D -182°C, which has been called collutine, has been isolated from the epigeal parts ofColchicum luteum Baker. On the basis of UV, IR, NMR, and mass spectra and chemical reactions, the structure of 4-hydroxy-2,3, 6-trimethoxyhomomorphinandienone has been proposed for collutine.
abstractGer	Summary A new base with the composition $ C_{21} %$ H_{25} %$ O_{5} $N, mp 192–194°C, [α]D -182°C, which has been called collutine, has been isolated from the epigeal parts ofColchicum luteum Baker. On the basis of UV, IR, NMR, and mass spectra and chemical reactions, the structure of 4-hydroxy-2,3, 6-trimethoxyhomomorphinandienone has been proposed for collutine.
abstract_unstemmed	Summary A new base with the composition $ C_{21} %$ H_{25} %$ O_{5} $N, mp 192–194°C, [α]D -182°C, which has been called collutine, has been isolated from the epigeal parts ofColchicum luteum Baker. On the basis of UV, IR, NMR, and mass spectra and chemical reactions, the structure of 4-hydroxy-2,3, 6-trimethoxyhomomorphinandienone has been proposed for collutine.
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container_issue	6
title_short	Structure and absolute configuration of collutine
url	https://dx.doi.org/10.1007/BF00568470
remote_bool	true
author2	Yusupov, M. K. Aslanov, Kh. A. Sadykov, A. S.
author2Str	Yusupov, M. K. Aslanov, Kh. A. Sadykov, A. S.
ppnlink	325568618
mediatype_str_mv	c
isOA_txt	false
hochschulschrift_bool	false
doi_str	10.1007/BF00568470
up_date	2024-07-04T00:03:43.848Z
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Structure and absolute configuration of collutine

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