A direct and simple approach for the synthesis of indole-3-propanol and its acetates from dihydropyran
Abstract A general method was developed for the one-pot synthesis of highly functionalized indoles from simple, commercially available phenylhydrazine hydrochlorides and dihydropyran. Synthesis of indole-3-propanol and its acetates was studied extensively for appropriate acetic acid and water mixtur...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Srinivasa, Aswathanarayana [verfasserIn] Mahadevan, Kittappa M. [verfasserIn] Sureshakumara, Tholappanavara H. [verfasserIn] Hulikal, Vijaykumar [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2008 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Monatshefte für Chemie - Wien [u.a.] : Springer, 1880, 139(2008), 12 vom: 09. Juni |
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| Übergeordnetes Werk: |
volume:139 ; year:2008 ; number:12 ; day:09 ; month:06 |
| Links: |
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| DOI / URN: |
10.1007/s00706-008-0945-x |
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| Katalog-ID: |
SPR007456263 |
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| 100 | 1 | |a Srinivasa, Aswathanarayana |e verfasserin |4 aut | |
| 245 | 1 | 2 | |a A direct and simple approach for the synthesis of indole-3-propanol and its acetates from dihydropyran |
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| 520 | |a Abstract A general method was developed for the one-pot synthesis of highly functionalized indoles from simple, commercially available phenylhydrazine hydrochlorides and dihydropyran. Synthesis of indole-3-propanol and its acetates was studied extensively for appropriate acetic acid and water mixture as the solvent. | ||
| 650 | 4 | |a Indole-3-propanol; Indole-3-propyl acetate; Acetic acid; Phenylhydrazine hydrochloride; Dihydropyran. |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Mahadevan, Kittappa M. |e verfasserin |4 aut | |
| 700 | 1 | |a Sureshakumara, Tholappanavara H. |e verfasserin |4 aut | |
| 700 | 1 | |a Hulikal, Vijaykumar |e verfasserin |4 aut | |
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2008 |
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35.00 |
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2008 |
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10.1007/s00706-008-0945-x doi (DE-627)SPR007456263 (SPR)s00706-008-0945-x-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Srinivasa, Aswathanarayana verfasserin aut A direct and simple approach for the synthesis of indole-3-propanol and its acetates from dihydropyran 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A general method was developed for the one-pot synthesis of highly functionalized indoles from simple, commercially available phenylhydrazine hydrochlorides and dihydropyran. Synthesis of indole-3-propanol and its acetates was studied extensively for appropriate acetic acid and water mixture as the solvent. Indole-3-propanol; Indole-3-propyl acetate; Acetic acid; Phenylhydrazine hydrochloride; Dihydropyran. (dpeaa)DE-He213 Mahadevan, Kittappa M. verfasserin aut Sureshakumara, Tholappanavara H. verfasserin aut Hulikal, Vijaykumar verfasserin aut Enthalten in Monatshefte für Chemie Wien [u.a.] : Springer, 1880 139(2008), 12 vom: 09. Juni (DE-627)25462992X (DE-600)1462037-6 1434-4475 nnns volume:139 year:2008 number:12 day:09 month:06 https://dx.doi.org/10.1007/s00706-008-0945-x 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_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 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_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 139 2008 12 09 06 |
| spelling |
10.1007/s00706-008-0945-x doi (DE-627)SPR007456263 (SPR)s00706-008-0945-x-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Srinivasa, Aswathanarayana verfasserin aut A direct and simple approach for the synthesis of indole-3-propanol and its acetates from dihydropyran 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A general method was developed for the one-pot synthesis of highly functionalized indoles from simple, commercially available phenylhydrazine hydrochlorides and dihydropyran. Synthesis of indole-3-propanol and its acetates was studied extensively for appropriate acetic acid and water mixture as the solvent. Indole-3-propanol; Indole-3-propyl acetate; Acetic acid; Phenylhydrazine hydrochloride; Dihydropyran. (dpeaa)DE-He213 Mahadevan, Kittappa M. verfasserin aut Sureshakumara, Tholappanavara H. verfasserin aut Hulikal, Vijaykumar verfasserin aut Enthalten in Monatshefte für Chemie Wien [u.a.] : Springer, 1880 139(2008), 12 vom: 09. Juni (DE-627)25462992X (DE-600)1462037-6 1434-4475 nnns volume:139 year:2008 number:12 day:09 month:06 https://dx.doi.org/10.1007/s00706-008-0945-x 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_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 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_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 139 2008 12 09 06 |
| allfields_unstemmed |
10.1007/s00706-008-0945-x doi (DE-627)SPR007456263 (SPR)s00706-008-0945-x-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Srinivasa, Aswathanarayana verfasserin aut A direct and simple approach for the synthesis of indole-3-propanol and its acetates from dihydropyran 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A general method was developed for the one-pot synthesis of highly functionalized indoles from simple, commercially available phenylhydrazine hydrochlorides and dihydropyran. Synthesis of indole-3-propanol and its acetates was studied extensively for appropriate acetic acid and water mixture as the solvent. Indole-3-propanol; Indole-3-propyl acetate; Acetic acid; Phenylhydrazine hydrochloride; Dihydropyran. (dpeaa)DE-He213 Mahadevan, Kittappa M. verfasserin aut Sureshakumara, Tholappanavara H. verfasserin aut Hulikal, Vijaykumar verfasserin aut Enthalten in Monatshefte für Chemie Wien [u.a.] : Springer, 1880 139(2008), 12 vom: 09. Juni (DE-627)25462992X (DE-600)1462037-6 1434-4475 nnns volume:139 year:2008 number:12 day:09 month:06 https://dx.doi.org/10.1007/s00706-008-0945-x 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_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 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_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 139 2008 12 09 06 |
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10.1007/s00706-008-0945-x doi (DE-627)SPR007456263 (SPR)s00706-008-0945-x-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Srinivasa, Aswathanarayana verfasserin aut A direct and simple approach for the synthesis of indole-3-propanol and its acetates from dihydropyran 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A general method was developed for the one-pot synthesis of highly functionalized indoles from simple, commercially available phenylhydrazine hydrochlorides and dihydropyran. Synthesis of indole-3-propanol and its acetates was studied extensively for appropriate acetic acid and water mixture as the solvent. Indole-3-propanol; Indole-3-propyl acetate; Acetic acid; Phenylhydrazine hydrochloride; Dihydropyran. (dpeaa)DE-He213 Mahadevan, Kittappa M. verfasserin aut Sureshakumara, Tholappanavara H. verfasserin aut Hulikal, Vijaykumar verfasserin aut Enthalten in Monatshefte für Chemie Wien [u.a.] : Springer, 1880 139(2008), 12 vom: 09. Juni (DE-627)25462992X (DE-600)1462037-6 1434-4475 nnns volume:139 year:2008 number:12 day:09 month:06 https://dx.doi.org/10.1007/s00706-008-0945-x 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_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 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_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 139 2008 12 09 06 |
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10.1007/s00706-008-0945-x doi (DE-627)SPR007456263 (SPR)s00706-008-0945-x-e DE-627 ger DE-627 rakwb eng 540 ASE 35.00 bkl Srinivasa, Aswathanarayana verfasserin aut A direct and simple approach for the synthesis of indole-3-propanol and its acetates from dihydropyran 2008 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract A general method was developed for the one-pot synthesis of highly functionalized indoles from simple, commercially available phenylhydrazine hydrochlorides and dihydropyran. Synthesis of indole-3-propanol and its acetates was studied extensively for appropriate acetic acid and water mixture as the solvent. Indole-3-propanol; Indole-3-propyl acetate; Acetic acid; Phenylhydrazine hydrochloride; Dihydropyran. (dpeaa)DE-He213 Mahadevan, Kittappa M. verfasserin aut Sureshakumara, Tholappanavara H. verfasserin aut Hulikal, Vijaykumar verfasserin aut Enthalten in Monatshefte für Chemie Wien [u.a.] : Springer, 1880 139(2008), 12 vom: 09. Juni (DE-627)25462992X (DE-600)1462037-6 1434-4475 nnns volume:139 year:2008 number:12 day:09 month:06 https://dx.doi.org/10.1007/s00706-008-0945-x 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_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 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_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 139 2008 12 09 06 |
| language |
English |
| source |
Enthalten in Monatshefte für Chemie 139(2008), 12 vom: 09. Juni volume:139 year:2008 number:12 day:09 month:06 |
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Enthalten in Monatshefte für Chemie 139(2008), 12 vom: 09. Juni volume:139 year:2008 number:12 day:09 month:06 |
| format_phy_str_mv |
Article |
| institution |
findex.gbv.de |
| topic_facet |
Indole-3-propanol; Indole-3-propyl acetate; Acetic acid; Phenylhydrazine hydrochloride; Dihydropyran. |
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540 |
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false |
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Monatshefte für Chemie |
| authorswithroles_txt_mv |
Srinivasa, Aswathanarayana @@aut@@ Mahadevan, Kittappa M. @@aut@@ Sureshakumara, Tholappanavara H. @@aut@@ Hulikal, Vijaykumar @@aut@@ |
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2008-06-09T00:00:00Z |
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25462992X |
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3540 |
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SPR007456263 |
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englisch |
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Srinivasa, Aswathanarayana |
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Srinivasa, Aswathanarayana ddc 540 bkl 35.00 misc Indole-3-propanol; Indole-3-propyl acetate; Acetic acid; Phenylhydrazine hydrochloride; Dihydropyran. A direct and simple approach for the synthesis of indole-3-propanol and its acetates from dihydropyran |
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540 ASE 35.00 bkl A direct and simple approach for the synthesis of indole-3-propanol and its acetates from dihydropyran Indole-3-propanol; Indole-3-propyl acetate; Acetic acid; Phenylhydrazine hydrochloride; Dihydropyran. (dpeaa)DE-He213 |
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ddc 540 bkl 35.00 misc Indole-3-propanol; Indole-3-propyl acetate; Acetic acid; Phenylhydrazine hydrochloride; Dihydropyran. |
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ddc 540 bkl 35.00 misc Indole-3-propanol; Indole-3-propyl acetate; Acetic acid; Phenylhydrazine hydrochloride; Dihydropyran. |
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A direct and simple approach for the synthesis of indole-3-propanol and its acetates from dihydropyran |
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direct and simple approach for the synthesis of indole-3-propanol and its acetates from dihydropyran |
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A direct and simple approach for the synthesis of indole-3-propanol and its acetates from dihydropyran |
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Abstract A general method was developed for the one-pot synthesis of highly functionalized indoles from simple, commercially available phenylhydrazine hydrochlorides and dihydropyran. Synthesis of indole-3-propanol and its acetates was studied extensively for appropriate acetic acid and water mixture as the solvent. |
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Abstract A general method was developed for the one-pot synthesis of highly functionalized indoles from simple, commercially available phenylhydrazine hydrochlorides and dihydropyran. Synthesis of indole-3-propanol and its acetates was studied extensively for appropriate acetic acid and water mixture as the solvent. |
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Abstract A general method was developed for the one-pot synthesis of highly functionalized indoles from simple, commercially available phenylhydrazine hydrochlorides and dihydropyran. Synthesis of indole-3-propanol and its acetates was studied extensively for appropriate acetic acid and water mixture as the solvent. |
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A direct and simple approach for the synthesis of indole-3-propanol and its acetates from dihydropyran |
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