Stereoselective synthesis of the naturally occurring 2-pyranone dodoneine
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Otros documentos de la autoría: Álvarez Bercedo, Paula; Falomir, Eva; Murga, Juan; Carda, Miguel; Marco, J. Alberto
Metadatos
Mostrar el registro completo del ítemcomunitat-uji-handle:10234/9
comunitat-uji-handle2:10234/7053
comunitat-uji-handle3:10234/8639
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Título
Stereoselective synthesis of the naturally occurring 2-pyranone dodoneineFecha de publicación
2008-08Editor
Wiley-VCHISSN
1434-193XCita bibliográfica
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. 4015-4018Tipo de documento
info:eu-repo/semantics/articlePalabras clave / Materias
Resumen
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 [-]
Publicado en
European journal of organic chemistry, 2008, no. 23Derechos de acceso
http://rightsstatements.org/vocab/CNE/1.0/
info:eu-repo/semantics/openAccess
info:eu-repo/semantics/openAccess
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