Detailed Information

Cited 0 time in webofscience Cited 0 time in scopus
Metadata Downloads

Intermolecular Double Prins-Type Cyclization: A Facile and Efficient Synthesis of 1,6-Dioxecanes

Full metadata record
DC Field Value Language
dc.contributor.authorUllapu, Punna Reddy-
dc.contributor.authorMin, Sun-Joon-
dc.contributor.authorChavre, Satish N.-
dc.contributor.authorChoo, Hyunah-
dc.contributor.authorLee, Jae Kyun-
dc.contributor.authorPae, Ae Nim-
dc.contributor.authorKim, Youseung-
dc.contributor.authorChang, Moon Ho-
dc.contributor.authorCho, Yong Seo-
dc.date.accessioned2021-06-23T16:38:41Z-
dc.date.available2021-06-23T16:38:41Z-
dc.date.issued2009-03-
dc.identifier.issn1433-7851-
dc.identifier.issn1521-3773-
dc.identifier.urihttps://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.extent5-
dc.language영어-
dc.language.isoENG-
dc.publisherJohn Wiley & Sons Ltd.-
dc.titleIntermolecular Double Prins-Type Cyclization: A Facile and Efficient Synthesis of 1,6-Dioxecanes-
dc.typeArticle-
dc.publisher.location독일-
dc.identifier.doi10.1002/anie.200804576-
dc.identifier.scopusid2-s2.0-61949133421-
dc.identifier.wosid000264411800031-
dc.identifier.bibliographicCitationAngewandte Chemie - International Edition, v.48, no.12, pp 2196 - 2200-
dc.citation.titleAngewandte Chemie - International Edition-
dc.citation.volume48-
dc.citation.number12-
dc.citation.startPage2196-
dc.citation.endPage2200-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusACID PROMOTED CYCLIZATION-
dc.subject.keywordPlusDIASTEREOSELECTIVE SYNTHESIS-
dc.subject.keywordPlusENANTIOSELECTIVE SYNTHESIS-
dc.subject.keywordPlusSTEREOSELECTIVE-SYNTHESIS-
dc.subject.keywordPlusREDUCTIVE CLEAVAGE-
dc.subject.keywordPlusRING-CLOSURE-
dc.subject.keywordPlusTETRAHYDROPYRANS-
dc.subject.keywordPlusACETALS-
dc.subject.keywordPlusETHERS-
dc.subject.keywordPlusTETRAHYDROFURAN-
dc.subject.keywordAuthorcyclization-
dc.subject.keywordAuthorDiels-Alder reaction-
dc.subject.keywordAuthorPrins-type reaction-
dc.subject.keywordAuthorsilanes-
dc.subject.keywordAuthorsynthetic methods-
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/10.1002/anie.200804576-
Files in This Item
Go to Link
Appears in
Collections
COLLEGE OF SCIENCE AND CONVERGENCE TECHNOLOGY > DEPARTMENT OF CHEMICAL AND MOLECULAR ENGINEERING > 1. Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Related Researcher

Researcher Min, Sun Joon photo

Min, Sun Joon
ERICA 공학대학 (ERICA 에너지바이오학과)
Read more

Altmetrics

Total Views & Downloads

BROWSE