Stereoselective synthesis of the naturally occurring 2-pyranone dodoneine
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Altres documents de l'autoria: Álvarez Bercedo, Paula; Falomir, Eva; Murga, Juan; Carda, Miguel; Marco, J. Alberto
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Mostra el registre complet de l'elementcomunitat-uji-handle:10234/9
comunitat-uji-handle2:10234/7053
comunitat-uji-handle3:10234/8639
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Títol
Stereoselective synthesis of the naturally occurring 2-pyranone dodoneineData de publicació
2008-08Editor
Wiley-VCHISSN
1434-193XCita bibliogràfica
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. 4015-4018Tipus de document
info:eu-repo/semantics/articleParaules clau / Matèries
Resum
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 [-]
Publicat a
European journal of organic chemistry, 2008, no. 23Drets d'accés
http://rightsstatements.org/vocab/CNE/1.0/
info:eu-repo/semantics/openAccess
info:eu-repo/semantics/openAccess
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