Intermolecular Double Prins-Type Cyclization: A Facile and Efficient Synthesis of 1,6-Dioxecanes
DC Field | Value | Language |
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dc.contributor.author | Ullapu, Punna Reddy | - |
dc.contributor.author | Min, Sun-Joon | - |
dc.contributor.author | Chavre, Satish N. | - |
dc.contributor.author | Choo, Hyunah | - |
dc.contributor.author | Lee, Jae Kyun | - |
dc.contributor.author | Pae, Ae Nim | - |
dc.contributor.author | Kim, Youseung | - |
dc.contributor.author | Chang, Moon Ho | - |
dc.contributor.author | Cho, Yong Seo | - |
dc.date.accessioned | 2021-06-23T16:38:41Z | - |
dc.date.available | 2021-06-23T16:38:41Z | - |
dc.date.issued | 2009-03 | - |
dc.identifier.issn | 1433-7851 | - |
dc.identifier.issn | 1521-3773 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/41770 | - |
dc.description.abstract | (Chemical Equation Presented) Double or nothing: The title reaction converts a range of aromatic aldehydes and allenylmethyl/allyl silanes into 1,6-dioxecane derivatives in good to excellent yields (see scheme; Ar=aryl, Tf=triflate, THF=tetrahydrofuran, TMS=trimethylsilyl). In addition, the bisdiene product has been transformed into the corresponding tricyclic compound through a Diels-Alder reaction. | - |
dc.format.extent | 5 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | John Wiley & Sons Ltd. | - |
dc.title | Intermolecular Double Prins-Type Cyclization: A Facile and Efficient Synthesis of 1,6-Dioxecanes | - |
dc.type | Article | - |
dc.publisher.location | 독일 | - |
dc.identifier.doi | 10.1002/anie.200804576 | - |
dc.identifier.scopusid | 2-s2.0-61949133421 | - |
dc.identifier.wosid | 000264411800031 | - |
dc.identifier.bibliographicCitation | Angewandte Chemie - International Edition, v.48, no.12, pp 2196 - 2200 | - |
dc.citation.title | Angewandte Chemie - International Edition | - |
dc.citation.volume | 48 | - |
dc.citation.number | 12 | - |
dc.citation.startPage | 2196 | - |
dc.citation.endPage | 2200 | - |
dc.type.docType | Article | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Multidisciplinary | - |
dc.subject.keywordPlus | ACID PROMOTED CYCLIZATION | - |
dc.subject.keywordPlus | DIASTEREOSELECTIVE SYNTHESIS | - |
dc.subject.keywordPlus | ENANTIOSELECTIVE SYNTHESIS | - |
dc.subject.keywordPlus | STEREOSELECTIVE-SYNTHESIS | - |
dc.subject.keywordPlus | REDUCTIVE CLEAVAGE | - |
dc.subject.keywordPlus | RING-CLOSURE | - |
dc.subject.keywordPlus | TETRAHYDROPYRANS | - |
dc.subject.keywordPlus | ACETALS | - |
dc.subject.keywordPlus | ETHERS | - |
dc.subject.keywordPlus | TETRAHYDROFURAN | - |
dc.subject.keywordAuthor | cyclization | - |
dc.subject.keywordAuthor | Diels-Alder reaction | - |
dc.subject.keywordAuthor | Prins-type reaction | - |
dc.subject.keywordAuthor | silanes | - |
dc.subject.keywordAuthor | synthetic methods | - |
dc.identifier.url | https://onlinelibrary.wiley.com/doi/10.1002/anie.200804576 | - |
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