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research article

A short synthesis of (-)-deoxoprosophylline

Jourdant, Angelique
•
Zhu, Jieping  
2004
Heterocycles

Syntheses of (-)-deoxoprosophylline from chiral L-N,N-di(benzyl)serine (TBDMS) aldehyde is reported. A highly diastereoselective nucleophilic addn. of Buechi's Grignard reagent to chiral serinal followed by an intramol. reductive amination of w-oxo amino diol are two key steps of the present synthesis. The target compd. was (2S,3R,6R)-6-dodecyl-3-hydroxy-2-piperidinemethanol, which is related to the Prosopis africana piperidine alkaloid family. [on SciFinder (R)]

  • Details
  • Metrics
Type
research article
DOI
10.3987/COM-04-S(P)21
Author(s)
Jourdant, Angelique
Zhu, Jieping  
Date Issued

2004

Published in
Heterocycles
Volume

64

Start page

249

End page

259

Subjects

Onium compounds Role: RCT (Reactant)

•

SPN (Synthetic preparation)

•

PREP (Preparation)

•

RACT (Reactant or reagent) (iminium

•

cyclic; prepn. of (-)-deoxoprosophylline via nucleophilic addn. of Buechi's Grignard reagent to chiral serinal

•

intramol. reductive amination of w-oxo amino diol and formation of cyclic iminium intermediate as key synthetic steps); Alkaloids Role: SPN (Synthetic preparation)

•

PREP (Preparation) (piperidine; prepn. of (2S

•

3R

•

6R)-(dodecyl)(hydroxy)-2-piperidinemethanol [(-)-deoxoprosophylline

•

Prosopis alkaloid] using Buechi's Grignard reagent and [bis(phenylmethyl)amino][[(dimethylethyl)dimethylsilyl]oxy]propanal as starting materials); Asymmetric synthesis and induction (prepn. of (-)-deoxoprosophylline via diastereoselective nucleophilic addn. of Buechi's Grignard reagent to chiral serinal and intramol. reductive amination of w-oxo amino diol intermediate as key synthetic steps); Prosopis africana (prepn. of (2S

•

3R

•

6R)-(dodecyl)(hydroxy)-2-piperidinemethanol [(-)-deoxoprosophylline

•

Prosopis alkaloid] using Buechi's Grignard reagent and [bis(phenylmethyl)amino][[(dimethylethyl)dimethylsilyl]oxy]propanal as starting materials); Amination (reductive

•

stereoselective; prepn. of (-)-deoxoprosophylline via reductive amination using (+)-(amino)(phenyl)methoxyoctadecanone deriv. as synthetic intermediate)

•

deoxoprosophylline piperidinemethanol dodecyl hydroxy asym synthesis; reductive amination stereoselective amino hydroxy silyl octadecanone prepn deoxoprosophylline; Prosopis africana piperidine alkaloid deoxoprosophylline stereoselective reductive amination iminium

Note

CAN 142:374002

31-3

Alkaloids

Institut de Chimie des Substances Naturelles, CNRS,Gif-sur-Yvette,Fr.

Journal

written in English.

100-39-0 (Benzyl bromide) Role: RCT (Reactant), RACT (Reactant or reagent) (prepn. of (-)-deoxoprosophylline intermediate using benzyl bromide as starting material); 349556-02-1P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. of (-)-deoxoprosophylline using (+)-(amino)(phenyl)methoxyhexanal as synthetic intermediate); 305838-42-0P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. of (-)-deoxoprosophylline using (+)-(hydroxy)[(silyl)methyl]-1,3-dioxolane-2-butanamine as synthetic intermediate); 349555-96-0P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. of (-)-deoxoprosophylline using (+)-[(phenyl)methoxy][(silyl)methyl]-1,3-dioxolane-2-butanamine as synthetic intermediate); 849428-93-9P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. of (-)-deoxoprosophylline using (-)-(amino)(dodecyl)[(phenyl)methoxy]-1,3-dioxolanepentanol deriv. as synthetic intermediate); 849428-90-6P; 849428-91-7P; 849428-92-8P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. of (-)-deoxoprosophylline using (amino)(dodecyl)[(phenyl)methoxy]-1,3-dioxolanepentanol as synthetic intermediate); 349556-03-2P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. of (-)-deoxoprosophylline using (amino)(phenyl)methoxyoctadecanol deriv. as synthetic intermediate); 143-15-7 Role: RCT (Reactant), RACT (Reactant or reagent) (prepn. of (-)-deoxoprosophylline using (bromo)undecane as starting material); 18742-02-4 (2-(2-Bromoethyl)-1,3-dioxolane); 125654-82-2 ((S)-N,N-Dibenzyl-O-(tert-butyldimethylsilyl)serinal) Role: RCT (Reactant), RACT (Reactant or reagent) (prepn. of (-)-deoxoprosophylline using Buechi's Grignard reagent and [bis(phenylmethyl)amino][[(dimethylethyl)dimethylsilyl]oxy]propanal as starting materials); 849428-94-0P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. of (-)-deoxoprosophylline via intramol. reductive amination of (amino)(hydroxy)[(phenyl)methoxy]octadecanone as key synthetic step); 349556-00-9P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. of (-)-deoxoprosophylline via stereoselective reductive amination using (+)-(amino)(phenyl)methoxyoctadecanone deriv. as synthetic intermediate); 849428-89-3P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. of (2S,3R,6R)-(dodecyl)(hydroxy)-2-piperidinemethanol [(-)-deoxoprosophylline] using Buechi's Grignard reagent and [bis(phenylmethyl)amino][[(dimethylethyl)dimethylsilyl]oxy]propanal as starting materials); 74843-69-9P ((-)-Deoxoprosophylline) Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of (2S,3R,6R)-(dodecyl)(hydroxy)-2-piperidinemethanol [(-)-deoxoprosophylline] using Buechi's Grignard reagent and [bis(phenylmethyl)amino][[(dimethylethyl)dimethylsilyl]oxy]propanal as starting materials)

Editorial or Peer reviewed

REVIEWED

Written at

OTHER

EPFL units
LSPN  
Available on Infoscience
November 25, 2010
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/58478
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