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- Publisher Website: 10.1055/s-2005-872077
- Scopus: eid_2-s2.0-26844510768
- WOS: WOS:000232503200014
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Article: Base-catalyzed, efficient synthesis of 5-substituted 3,6-dihydro-7H-1,2,3- triazolo[4,5-d]pyrimidin-7-ones
Title | Base-catalyzed, efficient synthesis of 5-substituted 3,6-dihydro-7H-1,2,3- triazolo[4,5-d]pyrimidin-7-ones |
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Authors | |
Keywords | Aza-Wittig Reactions Cyclizations Guanines Heterocycles Imides Pyrimidines |
Issue Date | 2005 |
Publisher | Georg Thieme Verlag. The Journal's web site is located at www.thieme-chemistry.com |
Citation | Synthesis, 2005 n. 15, p. 2544-2548 How to Cite? |
Abstract | The carbodiimides 2, obtained from aza-Wittig reactions of iminophosphorane 1 with aromatic isocyanates, reacted with secondary amines or ROH to give 5-dialkylamino or 5-alkoxy 7H-1,2,3-triazolo[4,5-d]pyrimidin-7-ones 4 in the presence of a catalytic amount of EtONa in a mixed solvent (CH 2Cl2-ROH). Reactions of 2 with phenols in presence of catalytic potassium carbonate in MeCN gave 5-aryloxy-7H-1,2,3-triazolo[4,5-d] pyrimidin-7-ones 4 in satisfactory yields. © Georg Thieme Verlag Stuttgart. |
Persistent Identifier | http://hdl.handle.net/10722/182327 |
ISSN | 2023 Impact Factor: 2.2 2023 SCImago Journal Rankings: 0.582 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Zhao, JF | en_US |
dc.contributor.author | Xie, C | en_US |
dc.contributor.author | Ding, MW | en_US |
dc.contributor.author | He, HW | en_US |
dc.date.accessioned | 2013-04-23T08:18:54Z | - |
dc.date.available | 2013-04-23T08:18:54Z | - |
dc.date.issued | 2005 | en_US |
dc.identifier.citation | Synthesis, 2005 n. 15, p. 2544-2548 | en_US |
dc.identifier.issn | 0039-7881 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/182327 | - |
dc.description.abstract | The carbodiimides 2, obtained from aza-Wittig reactions of iminophosphorane 1 with aromatic isocyanates, reacted with secondary amines or ROH to give 5-dialkylamino or 5-alkoxy 7H-1,2,3-triazolo[4,5-d]pyrimidin-7-ones 4 in the presence of a catalytic amount of EtONa in a mixed solvent (CH 2Cl2-ROH). Reactions of 2 with phenols in presence of catalytic potassium carbonate in MeCN gave 5-aryloxy-7H-1,2,3-triazolo[4,5-d] pyrimidin-7-ones 4 in satisfactory yields. © Georg Thieme Verlag Stuttgart. | en_US |
dc.language | eng | en_US |
dc.publisher | Georg Thieme Verlag. The Journal's web site is located at www.thieme-chemistry.com | en_US |
dc.relation.ispartof | Synthesis | en_US |
dc.subject | Aza-Wittig Reactions | en_US |
dc.subject | Cyclizations | en_US |
dc.subject | Guanines | en_US |
dc.subject | Heterocycles | en_US |
dc.subject | Imides | en_US |
dc.subject | Pyrimidines | en_US |
dc.title | Base-catalyzed, efficient synthesis of 5-substituted 3,6-dihydro-7H-1,2,3- triazolo[4,5-d]pyrimidin-7-ones | en_US |
dc.type | Article | en_US |
dc.identifier.email | Zhao, JF: zhao0065@e.ntu.edu.sg | en_US |
dc.identifier.authority | Zhao, JF=rp01745 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1055/s-2005-872077 | en_US |
dc.identifier.scopus | eid_2-s2.0-26844510768 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-26844510768&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.issue | 15 | en_US |
dc.identifier.spage | 2544 | en_US |
dc.identifier.epage | 2548 | en_US |
dc.identifier.isi | WOS:000232503200014 | - |
dc.publisher.place | Germany | en_US |
dc.identifier.scopusauthorid | Zhao, JF=8393022100 | en_US |
dc.identifier.scopusauthorid | Xie, C=35099729800 | en_US |
dc.identifier.scopusauthorid | Ding, MW=7202280967 | en_US |
dc.identifier.scopusauthorid | He, HW=7402291797 | en_US |
dc.identifier.issnl | 0039-7881 | - |