Stereoselective synthesis of the naturally occurring 2-pyranone dodoneine
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Other documents of the author: Álvarez Bercedo, Paula; Falomir, Eva; Murga, Juan; Carda, Miguel; Marco, J. Alberto
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comunitat-uji-handle2:10234/7053
comunitat-uji-handle3:10234/8639
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Title
Stereoselective synthesis of the naturally occurring 2-pyranone dodoneineDate
2008-08Publisher
Wiley-VCHISSN
1434-193XBibliographic citation
ÁLVAREZ BERCEDO, Laura; FALOMIR, Eva; MURGA, Juan; CARDA, Miguel; MARCO, J. Alberto. Stereoselective synthesis of the naturally occurring 2-pyranone dodoneine. European journal of organic chemistry, 2008, no. 23, p. 4015-4018Type
info:eu-repo/semantics/articleSubject
Abstract
The first total synthesis of the naturally occurring dihydropyranone dodoneine is reported. Asymmetric allylations were
used for the stereoselective generation of the two stereogenic centers. The pyranone ring was ... [+]
The first total synthesis of the naturally occurring dihydropyranone dodoneine is reported. Asymmetric allylations were
used for the stereoselective generation of the two stereogenic centers. The pyranone ring was created by means of a ringclosing
metathesis [-]
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European journal of organic chemistry, 2008, no. 23Rights
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info:eu-repo/semantics/openAccess
info:eu-repo/semantics/openAccess
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