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

Pilar Blanco; Felix Busqué; Pedro De March; Marta Figueredo; Josep Font; Elena Sanfeliu

doi:10.1002/ejoc.200300474

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

Pilar Blanco, Felix Busqué, Pedro De March, Marta Figueredo, Josep Font, Elena Sanfeliu

Department of Chemistry

Research output: Contribution to journal › Article › Research › peer-review

13 Citations (Scopus)

Abstract

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.

Original language	English
Pages (from-to)	48-53
Journal	European Journal of Organic Chemistry
Issue number	1
DOIs	https://doi.org/10.1002/ejoc.200300474
Publication status	Published - 1 Jan 2004

Keywords

Alkaloids
Configurational stability
Total synthesis

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10.1002/ejoc.200300474

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abstract = "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. {\textcopyright} Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.",

keywords = "Alkaloids, Configurational stability, Total synthesis",

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AU - Blanco, Pilar

AU - Busqué, Felix

AU - De March, Pedro

AU - Figueredo, Marta

AU - Font, Josep

AU - Sanfeliu, Elena

PY - 2004/1/1

Y1 - 2004/1/1

N2 - 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.

AB - 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.

KW - Alkaloids

KW - Configurational stability

KW - Total synthesis

U2 - 10.1002/ejoc.200300474

DO - 10.1002/ejoc.200300474

M3 - Article

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EP - 53

IS - 1

ER -

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

Abstract

Keywords

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