dc.contributor.author
Duda, Blazej
dc.contributor.author
Lentz, Dieter
dc.date.accessioned
2018-06-08T03:25:45Z
dc.date.available
2015-12-21T11:10:52.289Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/15164
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-19352
dc.description.abstract
F5S–C[triple bond, length as m-dash]C–CF3 can be easily prepared in high
yields in two steps from 3,3,3-trifluoropropyne. It is a powerful, versatile
dienophile in Diels–Alder reactions. Reactions at room temperature provide the
corresponding products in up to quantitative yields allowing the introduction
of the pentafluorosulfanyl group and trifluoromethyl group at the 1,2 position
en
dc.format.extent
4 Seiten
dc.rights.uri
http://creativecommons.org/licenses/by-nc/3.0/
dc.subject.ddc
500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie::572 Biochemie
dc.title
Simultaneous introduction of trifluoromethyl and λ6-pentafluorosulfanyl
substituents using F5S–C[triple bond, length as m-dash]C–CF3 as a dienophile
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation
Org. Biomol. Chem., 2015,13, 5625-5628
dcterms.bibliographicCitation.doi
10.1039/C5OB00610D
dcterms.bibliographicCitation.url
http://pubs.rsc.org/EN/content/articlepdf/2015/ob/c5ob00610d
refubium.affiliation
Biologie, Chemie, Pharmazie
de
refubium.funding
OpenAccess Publikation in Allianzlizenz
refubium.funding.id
Au-015061
refubium.mycore.fudocsId
FUDOCS_document_000000023647
refubium.resourceType.isindependentpub
no
refubium.mycore.derivateId
FUDOCS_derivate_000000005796
dcterms.accessRights.openaire
open access
