RuCl3/Oxone: An efficient combination for the synthesis of 3-aryl-[1,2,4]triazolo[4,3-a]pyridines from 2-(2-arylidenehydrazinol)pyridines
An efficient and convenient method for the synthesis of 3-aryl[1,2,4]triazolo[4,3-a]pyridines has been developed involving RuCl3/Oxone-oxidative cyclization of 2-(2-arylidenehydrazinyl)pyridines, which occurs chemoselectively at the pyridine nitrogen. RuCl3 can be used as an efficient catalyst for t...
Ausführliche Beschreibung
Autor*in: |
Swamy, Tallapally [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2016 |
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Umfang: |
3 |
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Übergeordnetes Werk: |
Enthalten in: Continuing Medical Education Program - 2013, Amsterdam [u.a.] |
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Übergeordnetes Werk: |
volume:57 ; year:2016 ; number:50 ; day:14 ; month:12 ; pages:5596-5598 ; extent:3 |
Links: |
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DOI / URN: |
10.1016/j.tetlet.2016.10.110 |
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ELV024132551 |
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10.1016/j.tetlet.2016.10.110 doi GBV00000000000050A.pica (DE-627)ELV024132551 (ELSEVIER)S0040-4039(16)31443-5 DE-627 ger DE-627 rakwb eng 540 540 DE-600 610 VZ 540 VZ 35.00 bkl Swamy, Tallapally verfasserin aut RuCl3/Oxone: An efficient combination for the synthesis of 3-aryl-[1,2,4]triazolo[4,3-a]pyridines from 2-(2-arylidenehydrazinol)pyridines 2016 3 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier An efficient and convenient method for the synthesis of 3-aryl[1,2,4]triazolo[4,3-a]pyridines has been developed involving RuCl3/Oxone-oxidative cyclization of 2-(2-arylidenehydrazinyl)pyridines, which occurs chemoselectively at the pyridine nitrogen. RuCl3 can be used as an efficient catalyst for the synthesis of triazolopyridines through a direct intramolecular cyclization involving CN bond formation. Triazolopyridines Elsevier Intramolecular cyclization Elsevier Chemoselectively Elsevier 2-(2-Arylidenehydrazinyl)pyridines Elsevier Oxidative cyclization Elsevier RuCl3/Oxone Elsevier Raviteja, Padma oth Srikanth, Goskula oth Reddy, Basi V. Subba oth Ravinder, Vadde oth Enthalten in Elsevier Science Continuing Medical Education Program 2013 Amsterdam [u.a.] (DE-627)ELV011942339 volume:57 year:2016 number:50 day:14 month:12 pages:5596-5598 extent:3 https://doi.org/10.1016/j.tetlet.2016.10.110 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 35.00 Chemie: Allgemeines VZ AR 57 2016 50 14 1214 5596-5598 3 045F 540 |
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10.1016/j.tetlet.2016.10.110 doi GBV00000000000050A.pica (DE-627)ELV024132551 (ELSEVIER)S0040-4039(16)31443-5 DE-627 ger DE-627 rakwb eng 540 540 DE-600 610 VZ 540 VZ 35.00 bkl Swamy, Tallapally verfasserin aut RuCl3/Oxone: An efficient combination for the synthesis of 3-aryl-[1,2,4]triazolo[4,3-a]pyridines from 2-(2-arylidenehydrazinol)pyridines 2016 3 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier An efficient and convenient method for the synthesis of 3-aryl[1,2,4]triazolo[4,3-a]pyridines has been developed involving RuCl3/Oxone-oxidative cyclization of 2-(2-arylidenehydrazinyl)pyridines, which occurs chemoselectively at the pyridine nitrogen. RuCl3 can be used as an efficient catalyst for the synthesis of triazolopyridines through a direct intramolecular cyclization involving CN bond formation. Triazolopyridines Elsevier Intramolecular cyclization Elsevier Chemoselectively Elsevier 2-(2-Arylidenehydrazinyl)pyridines Elsevier Oxidative cyclization Elsevier RuCl3/Oxone Elsevier Raviteja, Padma oth Srikanth, Goskula oth Reddy, Basi V. Subba oth Ravinder, Vadde oth Enthalten in Elsevier Science Continuing Medical Education Program 2013 Amsterdam [u.a.] (DE-627)ELV011942339 volume:57 year:2016 number:50 day:14 month:12 pages:5596-5598 extent:3 https://doi.org/10.1016/j.tetlet.2016.10.110 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 35.00 Chemie: Allgemeines VZ AR 57 2016 50 14 1214 5596-5598 3 045F 540 |
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10.1016/j.tetlet.2016.10.110 doi GBV00000000000050A.pica (DE-627)ELV024132551 (ELSEVIER)S0040-4039(16)31443-5 DE-627 ger DE-627 rakwb eng 540 540 DE-600 610 VZ 540 VZ 35.00 bkl Swamy, Tallapally verfasserin aut RuCl3/Oxone: An efficient combination for the synthesis of 3-aryl-[1,2,4]triazolo[4,3-a]pyridines from 2-(2-arylidenehydrazinol)pyridines 2016 3 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier An efficient and convenient method for the synthesis of 3-aryl[1,2,4]triazolo[4,3-a]pyridines has been developed involving RuCl3/Oxone-oxidative cyclization of 2-(2-arylidenehydrazinyl)pyridines, which occurs chemoselectively at the pyridine nitrogen. RuCl3 can be used as an efficient catalyst for the synthesis of triazolopyridines through a direct intramolecular cyclization involving CN bond formation. Triazolopyridines Elsevier Intramolecular cyclization Elsevier Chemoselectively Elsevier 2-(2-Arylidenehydrazinyl)pyridines Elsevier Oxidative cyclization Elsevier RuCl3/Oxone Elsevier Raviteja, Padma oth Srikanth, Goskula oth Reddy, Basi V. Subba oth Ravinder, Vadde oth Enthalten in Elsevier Science Continuing Medical Education Program 2013 Amsterdam [u.a.] (DE-627)ELV011942339 volume:57 year:2016 number:50 day:14 month:12 pages:5596-5598 extent:3 https://doi.org/10.1016/j.tetlet.2016.10.110 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 35.00 Chemie: Allgemeines VZ AR 57 2016 50 14 1214 5596-5598 3 045F 540 |
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10.1016/j.tetlet.2016.10.110 doi GBV00000000000050A.pica (DE-627)ELV024132551 (ELSEVIER)S0040-4039(16)31443-5 DE-627 ger DE-627 rakwb eng 540 540 DE-600 610 VZ 540 VZ 35.00 bkl Swamy, Tallapally verfasserin aut RuCl3/Oxone: An efficient combination for the synthesis of 3-aryl-[1,2,4]triazolo[4,3-a]pyridines from 2-(2-arylidenehydrazinol)pyridines 2016 3 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier An efficient and convenient method for the synthesis of 3-aryl[1,2,4]triazolo[4,3-a]pyridines has been developed involving RuCl3/Oxone-oxidative cyclization of 2-(2-arylidenehydrazinyl)pyridines, which occurs chemoselectively at the pyridine nitrogen. RuCl3 can be used as an efficient catalyst for the synthesis of triazolopyridines through a direct intramolecular cyclization involving CN bond formation. Triazolopyridines Elsevier Intramolecular cyclization Elsevier Chemoselectively Elsevier 2-(2-Arylidenehydrazinyl)pyridines Elsevier Oxidative cyclization Elsevier RuCl3/Oxone Elsevier Raviteja, Padma oth Srikanth, Goskula oth Reddy, Basi V. Subba oth Ravinder, Vadde oth Enthalten in Elsevier Science Continuing Medical Education Program 2013 Amsterdam [u.a.] (DE-627)ELV011942339 volume:57 year:2016 number:50 day:14 month:12 pages:5596-5598 extent:3 https://doi.org/10.1016/j.tetlet.2016.10.110 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 35.00 Chemie: Allgemeines VZ AR 57 2016 50 14 1214 5596-5598 3 045F 540 |
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10.1016/j.tetlet.2016.10.110 doi GBV00000000000050A.pica (DE-627)ELV024132551 (ELSEVIER)S0040-4039(16)31443-5 DE-627 ger DE-627 rakwb eng 540 540 DE-600 610 VZ 540 VZ 35.00 bkl Swamy, Tallapally verfasserin aut RuCl3/Oxone: An efficient combination for the synthesis of 3-aryl-[1,2,4]triazolo[4,3-a]pyridines from 2-(2-arylidenehydrazinol)pyridines 2016 3 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier An efficient and convenient method for the synthesis of 3-aryl[1,2,4]triazolo[4,3-a]pyridines has been developed involving RuCl3/Oxone-oxidative cyclization of 2-(2-arylidenehydrazinyl)pyridines, which occurs chemoselectively at the pyridine nitrogen. RuCl3 can be used as an efficient catalyst for the synthesis of triazolopyridines through a direct intramolecular cyclization involving CN bond formation. Triazolopyridines Elsevier Intramolecular cyclization Elsevier Chemoselectively Elsevier 2-(2-Arylidenehydrazinyl)pyridines Elsevier Oxidative cyclization Elsevier RuCl3/Oxone Elsevier Raviteja, Padma oth Srikanth, Goskula oth Reddy, Basi V. Subba oth Ravinder, Vadde oth Enthalten in Elsevier Science Continuing Medical Education Program 2013 Amsterdam [u.a.] (DE-627)ELV011942339 volume:57 year:2016 number:50 day:14 month:12 pages:5596-5598 extent:3 https://doi.org/10.1016/j.tetlet.2016.10.110 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 35.00 Chemie: Allgemeines VZ AR 57 2016 50 14 1214 5596-5598 3 045F 540 |
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RuCl3/Oxone: An efficient combination for the synthesis of 3-aryl-[1,2,4]triazolo[4,3-a]pyridines from 2-(2-arylidenehydrazinol)pyridines |
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rucl3/oxone: an efficient combination for the synthesis of 3-aryl-[1,2,4]triazolo[4,3-a]pyridines from 2-(2-arylidenehydrazinol)pyridines |
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RuCl3/Oxone: An efficient combination for the synthesis of 3-aryl-[1,2,4]triazolo[4,3-a]pyridines from 2-(2-arylidenehydrazinol)pyridines |
abstract |
An efficient and convenient method for the synthesis of 3-aryl[1,2,4]triazolo[4,3-a]pyridines has been developed involving RuCl3/Oxone-oxidative cyclization of 2-(2-arylidenehydrazinyl)pyridines, which occurs chemoselectively at the pyridine nitrogen. RuCl3 can be used as an efficient catalyst for the synthesis of triazolopyridines through a direct intramolecular cyclization involving CN bond formation. |
abstractGer |
An efficient and convenient method for the synthesis of 3-aryl[1,2,4]triazolo[4,3-a]pyridines has been developed involving RuCl3/Oxone-oxidative cyclization of 2-(2-arylidenehydrazinyl)pyridines, which occurs chemoselectively at the pyridine nitrogen. RuCl3 can be used as an efficient catalyst for the synthesis of triazolopyridines through a direct intramolecular cyclization involving CN bond formation. |
abstract_unstemmed |
An efficient and convenient method for the synthesis of 3-aryl[1,2,4]triazolo[4,3-a]pyridines has been developed involving RuCl3/Oxone-oxidative cyclization of 2-(2-arylidenehydrazinyl)pyridines, which occurs chemoselectively at the pyridine nitrogen. RuCl3 can be used as an efficient catalyst for the synthesis of triazolopyridines through a direct intramolecular cyclization involving CN bond formation. |
collection_details |
GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA |
container_issue |
50 |
title_short |
RuCl3/Oxone: An efficient combination for the synthesis of 3-aryl-[1,2,4]triazolo[4,3-a]pyridines from 2-(2-arylidenehydrazinol)pyridines |
url |
https://doi.org/10.1016/j.tetlet.2016.10.110 |
remote_bool |
true |
author2 |
Raviteja, Padma Srikanth, Goskula Reddy, Basi V. Subba Ravinder, Vadde |
author2Str |
Raviteja, Padma Srikanth, Goskula Reddy, Basi V. Subba Ravinder, Vadde |
ppnlink |
ELV011942339 |
mediatype_str_mv |
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isOA_txt |
false |
hochschulschrift_bool |
false |
author2_role |
oth oth oth oth |
doi_str |
10.1016/j.tetlet.2016.10.110 |
up_date |
2024-07-06T20:37:58.643Z |
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1803863487827410944 |
fullrecord_marcxml |
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