Dergi makalesi Açık Erişim
Awheda, Ismail; Saygili, Nezire; Garner, A. Christopher; Wallis, John D.
{ "conceptrecid": "15110", "created": "2021-03-15T08:30:01.413159+00:00", "doi": "10.1039/c3ra41074a", "files": [ { "bucket": "ae27f05a-9ccb-404b-bb9f-42b6f98b2103", "checksum": "md5:4d50dc3047da9df3aa387850eed6e3e0", "key": "bib-afc56d45-bef3-415e-82a0-0f0256631dad.txt", "links": { "self": "https://aperta.ulakbim.gov.tr/api/files/ae27f05a-9ccb-404b-bb9f-42b6f98b2103/bib-afc56d45-bef3-415e-82a0-0f0256631dad.txt" }, "size": 187, "type": "txt" } ], "id": 15111, "links": { "badge": "https://aperta.ulakbim.gov.tr/badge/doi/10.1039/c3ra41074a.svg", "bucket": "https://aperta.ulakbim.gov.tr/api/files/ae27f05a-9ccb-404b-bb9f-42b6f98b2103", "doi": "https://doi.org/10.1039/c3ra41074a", "html": "https://aperta.ulakbim.gov.tr/record/15111", "latest": "https://aperta.ulakbim.gov.tr/api/records/15111", "latest_html": "https://aperta.ulakbim.gov.tr/record/15111" }, "metadata": { "access_right": "open", "access_right_category": "success", "communities": [ { "id": "tubitak-destekli-proje-yayinlari" } ], "creators": [ { "affiliation": "Nottingham Trent Univ, Sch Sci & Technol, Nottingham NG11 8NS, England", "name": "Awheda, Ismail" }, { "affiliation": "Hacettepe Univ, Fac Pharm, Dept Basic Pharmaceut Sci, TR-06100 Ankara, Turkey", "name": "Saygili, Nezire" }, { "affiliation": "Nottingham Trent Univ, Sch Sci & Technol, Nottingham NG11 8NS, England", "name": "Garner, A. Christopher" }, { "affiliation": "Nottingham Trent Univ, Sch Sci & Technol, Nottingham NG11 8NS, England", "name": "Wallis, John D." } ], "description": "The cyclic thionocarbamate of alaninol undergoes nucleophilic attack by sulfur nucleophiles at 5-C to give 1-thiopropyl-2-amine derivatives when derivatised on nitrogen with a Boc group. Iodide under microwave conditions causes a rearrangement to the isomeric thiazolidinone, while \"hard\" nucleophiles react at the thione group to yield a variety of product types by subsequent C-N or C-O cleavage. X-ray crystallography studies showed that the N-Boc group reduces delocalisation of electron density from nitrogen into the thione group, and thus promotes activation of the ring to nucleophilic attack.", "doi": "10.1039/c3ra41074a", "has_grant": false, "journal": { "issue": "47", "pages": "24997-25009", "title": "RSC ADVANCES", "volume": "3" }, "license": { "id": "cc-by" }, "publication_date": "2013-01-01", "relations": { "version": [ { "count": 1, "index": 0, "is_last": true, "last_child": { "pid_type": "recid", "pid_value": "15111" }, "parent": { "pid_type": "recid", "pid_value": "15110" } } ] }, "resource_type": { "subtype": "article", "title": "Dergi makalesi", "type": "publication" }, "title": "Activation and regioselectivity of five-membered cyclic thionocarbamates to nucleophilic attack" }, "owners": [ 1 ], "revision": 1, "stats": { "downloads": 4.0, "unique_downloads": 4.0, "unique_views": 36.0, "version_downloads": 4.0, "version_unique_downloads": 4.0, "version_unique_views": 36.0, "version_views": 36.0, "version_volume": 748.0, "views": 36.0, "volume": 748.0 }, "updated": "2021-03-15T08:30:01.461509+00:00" }
Görüntülenme | 36 |
İndirme | 4 |
Veri hacmi | 748 Bytes |
Tekil görüntülenme | 36 |
Tekil indirme | 4 |