Synthetic Studies on  Pandanus  Alkaloids: From Norpandamarilactonines to Pandamarilactonines, a Proof of Their Configurational Instability | Zendy

Blanco Pilar | Zendy; Busqué Felix | Zendy; de March Pedro | Zendy; Figueredo Marta | Zendy; Font Josep | Zendy; Sanfeliu Elena | Zendy

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Synthetic Studies on Pandanus Alkaloids: From Norpandamarilactonines to Pandamarilactonines, a Proof of Their Configurational Instability

Author(s) -

Blanco Pilar,

Busqué Felix,

de March Pedro,

Figueredo Marta,

Font Josep,

Sanfeliu Elena

Publication year - 2004

Publication title -

european journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.825

H-Index - 155

eISSN - 1099-0690

pISSN - 1434-193X

DOI - 10.1002/ejoc.200300474

Subject(s) - chemistry , diastereomer , amine gas treating , organic chemistry , stereochemistry , carbamate

The ethyl carbamate of norpandamarilactonine‐A was prepared in an enantiomerically pure form starting from ( S )‐prolinol. Deprotection of the amine functionality rendered both diastereomeric norpandamarilactonines as racemates, which were used as synthetic precursors of pandamarilactonine‐A and ‐B. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004)

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