Приказ основних података о документу

Expanding the scope of the indium-promoted allylation reaction: 4-(bromomethyl)-1,3-dioxol-2-one as a synthetic equivalent of a 3-arylhydroxyacetone enolate

dc.creatorBigović, Miljan
dc.creatorŠkaro, Sanja
dc.creatorMaslak, Veselin
dc.creatorSaičić, Radomir
dc.date.accessioned2018-11-22T00:24:26Z
dc.date.available2018-11-22T00:24:26Z
dc.date.issued2013
dc.identifier.issn0040-4039
dc.identifier.urihttps://cherry.chem.bg.ac.rs/handle/123456789/1430
dc.description.abstractCyclic enol carbonates of type 2, obtained via the indium-promoted allylation of aldehydes with 4-(bromomethyl)-1,3-dioxol-2-one, undergo Heck reaction with aryl iodides in the presence of silver trifluoroacetate, to give the corresponding arylated products. Thus, 4-(bromomethyl)-1,3-dioxol-2-one can be considered as a synthetic equivalent of 3-mylhydroxyacetone enolate.en
dc.publisherPergamon-Elsevier Science Ltd, Oxford
dc.rightsrestrictedAccess
dc.sourceTetrahedron Letters
dc.subjectAllylationen
dc.subjectIndiumen
dc.subjectHeck reactionen
dc.subjectAldol reactionen
dc.subjectOrganic synthesisen
dc.titleExpanding the scope of the indium-promoted allylation reaction: 4-(bromomethyl)-1,3-dioxol-2-one as a synthetic equivalent of a 3-arylhydroxyacetone enolateen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractБиговиц, Миљан; Маслак, Веселин; Саичић, Радомир; Скаро, Сања;
dc.citation.volume54
dc.citation.issue48
dc.citation.spage6624
dc.citation.epage6626
dc.identifier.wos000326613600054
dc.identifier.doi10.1016/j.tetlet.2013.09.115
dc.citation.other54(48): 6624-6626
dc.citation.rankM22
dc.description.otherSupplementary material: [http://cherry.chem.bg.ac.rs/handle/123456789/3493]
dc.type.versionpublishedVersionen
dc.identifier.scopus2-s2.0-84886791811


Документи

Thumbnail
Име:
1428.pdf
Величина:
2.233Mb
Формат:
PDF
Отварање

Овај документ се појављује у следећим колекцијама

Приказ основних података о документу