Yayın: Diverse Modes of Reactivity of 6-(Chloromethyl)-6-methylfulvene
| dc.contributor.author | Erdem, İhsan | |
| dc.contributor.author | Gronert, Scott | |
| dc.contributor.author | Cabrera, Gabriel | |
| dc.contributor.author | Tapken, Marco | |
| dc.contributor.buuauthor | Coşkun, Necdet | |
| dc.contributor.department | Fen Edebiyat Fakültesi | |
| dc.contributor.department | Kimya Bölümü | |
| dc.contributor.researcherid | B-1200-2012 | |
| dc.contributor.scopusid | 7004177880 | |
| dc.date.accessioned | 2023-08-15T06:54:37Z | |
| dc.date.available | 2023-08-15T06:54:37Z | |
| dc.date.issued | 2017-05-26 | |
| dc.description.abstract | The title compound exhibits a number of modes of reactivity toward nucleophiles/bases owing to the presence of several electrophilic and potentially nucleophilic sites in the molecule. We explored the reactions of 6-(chloromethyl)-6-methylfulvene with oxygen and nitrogen nucleophiles and bases as well as a carbon-based nucleophile (an enamine) and realized all possible reactivity modes predicted on the basis of electrophilic and nucleophilic positions in this compound. | |
| dc.description.sponsorship | United States Department of Health & Human Services National Institutes of Health (NIH) - USA - SC1 GM082340 | |
| dc.description.sponsorship | National Science Foundation (NSF) - CHE-1565852 - CHE-1228656 | |
| dc.description.sponsorship | United States Department of Health & Human Services National Institutes of Health (NIH) - USA - R25-GM059298 Appeared in source as:NIH MBRS-RISE scholarship | |
| dc.description.sponsorship | NIH-MS-PhD Bridge scholarship - R-25-GM048972 | |
| dc.description.sponsorship | National Science Foundation (NSF) NSF - Directorate for Mathematical & Physical Sciences (MPS) - 1565852 | |
| dc.identifier.citation | Erden, İ. vd. (2017). ''Diverse Modes of Reactivity of 6-(Chloromethyl)-6-methylfulvene''. European Journal of Organic Chemistry, 20(2017), 2925-2931. | |
| dc.identifier.doi | 10.1002/ejoc.201700442 | |
| dc.identifier.endpage | 2931 | |
| dc.identifier.issn | 1434-193X | |
| dc.identifier.issn | 1099-0690 | |
| dc.identifier.issue | 2017 | |
| dc.identifier.pubmed | 29200937 | |
| dc.identifier.scopus | 2-s2.0-85020045276 | |
| dc.identifier.startpage | 29525 | |
| dc.identifier.uri | https://doi.org/10.1002/ejoc.201700442 | |
| dc.identifier.uri | https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.201700442 | |
| dc.identifier.uri | http://hdl.handle.net/11452/33491 | |
| dc.identifier.volume | 20 | |
| dc.identifier.wos | 000403678500007 | |
| dc.indexed.wos | SCIE | |
| dc.indexed.wos | IC | |
| dc.language.iso | en | |
| dc.publisher | Wiley-V C H | |
| dc.relation.collaboration | Yurt dışı | |
| dc.relation.journal | European Journal of Organic Chemistry | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | |
| dc.relation.tubitak | BIDEP-2219 | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.subject | Chemistry | |
| dc.subject | Fulvenes | |
| dc.subject | Nucleophilic addition | |
| dc.subject | Cycloaddition | |
| dc.subject | 1,2-Dihydropentalene | |
| dc.subject | Reaction mechanisms | |
| dc.subject | Substituted fulvenes | |
| dc.subject | Cyclopentadiene | |
| dc.subject | Dimethylfulvene | |
| dc.subject | Cycloaddition | |
| dc.subject | 6,6-dimethylfulvene | |
| dc.subject | Elimination | |
| dc.subject | Precursors | |
| dc.subject | Products | |
| dc.subject | Acetone | |
| dc.subject | System | |
| dc.subject.scopus | Fulvene; Isomers; Cyclopropenone | |
| dc.subject.wos | Chemistry, organic | |
| dc.title | Diverse Modes of Reactivity of 6-(Chloromethyl)-6-methylfulvene | |
| dc.type | Article | |
| dc.wos.quartile | Q2 | |
| dspace.entity.type | Publication | |
| local.contributor.department | Fen Edebiyat Fakültesi/Kimya Bölümü | |
| local.indexed.at | Scopus | |
| local.indexed.at | WOS |
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