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  4. Asymmetric synthesis of orthogonally protected (2S,4R)- and (2S,4S)-4-hydroxyornithine
 
research article

Asymmetric synthesis of orthogonally protected (2S,4R)- and (2S,4S)-4-hydroxyornithine

Lepine, Renaud
•
Carbonnelle, Anny-Claude
•
Zhu, Jieping  
2003
Synlett

Synthesis of orthogonally protected (2S,4R)- and (2S,4S)-4-hydroxyornithines I is reported featuring an asym. alkylation of N-(diphenylmethylene)glycine tert-Bu ester with (5S)-N-benzyloxycarbonyl-5-iodomethyl oxazolidine. Double stereoselection was examd. using chiral ammonium salts as phase transfer catalysts, and a substrate-directed chiral induction is documented. [on SciFinder (R)]

  • Details
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Type
research article
DOI
10.1055/s-2003-40840
Author(s)
Lepine, Renaud
Carbonnelle, Anny-Claude
Zhu, Jieping  
Date Issued

2003

Published in
Synlett
Issue

10

Start page

1455

End page

1458

Subjects

Asymmetric synthesis and induction (asym. synthesis of orthogonally protected hydroxyornithines and their derivs.); Amino acids Role: SPN (Synthetic preparation)

•

PREP (Preparation) (esters; asym. synthesis of orthogonally protected hydroxyornithines and their derivs.)

•

ornithine hydroxy orthogonally protected asym synthesis

Note

CAN 140:16939

34-2

Amino Acids, Peptides, and Proteins

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

Journal

written in English.

61278-21-5P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (N-protection; asym. synthesis of orthogonally protected hydroxyornithines and their derivs.); 1643-19-2 (Tetrabutylammonium bromide); 200132-54-3; 219601-70-4; 534570-50-8 Role: CAT (Catalyst use), USES (Uses) (asym. synthesis of orthogonally protected hydroxyornithines and their derivs.); 630400-90-7P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (asym. synthesis of orthogonally protected hydroxyornithines and their derivs.); 329912-53-0P; 371972-14-4P; 630400-89-4P Role: SPN (Synthetic preparation), PREP (Preparation) (asym. synthesis of orthogonally protected hydroxyornithines and their derivs.); 23788-74-1P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (azidation; asym. synthesis of orthogonally protected hydroxyornithines and their derivs.); 81477-94-3 Role: RCT (Reactant), RACT (Reactant or reagent) (coupling with (iodomethyl)oxazolidine; asym. synthesis of orthogonally protected hydroxyornithines and their derivs.); 630400-88-3P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (coupling with imino ester; asym. synthesis of orthogonally protected hydroxyornithines and their derivs.); 630400-87-2P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (iodination; asym. synthesis of orthogonally protected hydroxyornithines and their derivs.); 135582-93-3P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (monotosylation; asym. synthesis of orthogonally protected hydroxyornithines and their derivs.); 630400-86-1P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (oxazolidine ring closure; asym. synthesis of orthogonally protected hydroxyornithines and their derivs.); 85820-82-2P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (redn./ring opening; asym. synthesis of orthogonally protected hydroxyornithines and their derivs.); 13139-17-8; 22323-82-6 Role: RCT (Reactant), RACT (Reactant or reagent) (tosylation; asym. synthesis of orthogonally protected hydroxyornithines and their derivs.)

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/20.500.14299/58489
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