dc.contributor.author | Katritzky, Alan R. | |
dc.contributor.author | Abdel-Fattah, Ashraf A. A. | |
dc.contributor.author | Çelik, İlhami | |
dc.date.accessioned | 2019-10-20T09:03:11Z | |
dc.date.available | 2019-10-20T09:03:11Z | |
dc.date.issued | 2007 | |
dc.identifier.issn | 1551-7004 | |
dc.identifier.issn | 1551-7012 | |
dc.identifier.uri | https://dx.doi.org/10.3998/ark.5550190.0008.b09 | |
dc.identifier.uri | https://hdl.handle.net/11421/16651 | |
dc.description | WOS: 000251573700010 | en_US |
dc.description.abstract | Reactions of readily available and stable N-(alpha-amidoalkyl)benzotriazoles 1 ( derived from a variety of aliphatic, aromatic or heterocyclic aldehydes) with diverse nitroalkanes, nitriles, alkynes and esters afforded N-(beta-nitroalkyl) amides 4 (54-96%), N-(beta-cyanoalkyl) amides 6 (58-88%), N- acylpropargylamines 11 (41-87%) and esters of beta-N-acylamino acids 13 (68-96%), respectively. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Arkat Usa Inc | en_US |
dc.relation.isversionof | 10.3998/ark.5550190.0008.b09 | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Amidoalkylation | en_US |
dc.subject | N-(Beta-Nitroalkyl) Amides | en_US |
dc.subject | N-(Beta-Cyanoalkyl)-Amides | en_US |
dc.subject | N-Acylpropargylamines | en_US |
dc.subject | Beta-N-Acylamino Acids | en_US |
dc.title | Benzotriazole-mediated amidoalkylations of nitroalkanes, nitriles, alkynes and esters | en_US |
dc.type | article | en_US |
dc.relation.journal | Arkivoc | en_US |
dc.contributor.department | Anadolu Üniversitesi, Fen Fakültesi, Fizik Bölümü | en_US |
dc.identifier.startpage | 96 | en_US |
dc.identifier.endpage | 113 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.contributor.institutionauthor | Çelik, İlhami | |