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  4. A New Approach to the Synthesis of Piperazinomycin and Bouvardin: Facile Access to Cycloisodityrosine via an Intramolecular SNAr Reaction
 
research article

A New Approach to the Synthesis of Piperazinomycin and Bouvardin: Facile Access to Cycloisodityrosine via an Intramolecular SNAr Reaction

Beugelmans, Rene
•
Bigot, Antony
•
Bois-Choussy, Michele
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1996
The Journal of Organic Chemistry

A new method for the synthesis of cycloisodityrosine atropisomers I (R1 = CO2Me, R2 = NHBoc), a 14-membered m,p-cyclophane, is reported. The synthesis hinged on an efficient macrocyclization procedure for biaryl ether formation based on an intramol. SNAr reaction. The cyclization conditions are much milder and the yield is much higher than those previously reported. Moreover, the presence of the NO2 function in I provides an opportunity to introduce not only the hydroxyl group found in natural products but also others such as amino acid amide for bioactivity evaluation. 3-Fluoro-4-nitrophenylalanine II was prepd. by alkylation of a chiral bislactim ether with 3-fluoro-4-nitrobenzyl bromide; secondary amine III resulting from the double alkylation was isolated as a minor product and characterized. A mechanism was proposed for its formation. [on SciFinder (R)]

  • Details
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Type
research article
DOI
10.1021/jo951375j
Author(s)
Beugelmans, Rene
Bigot, Antony
Bois-Choussy, Michele
Zhu, Jieping  
Date Issued

1996

Published in
The Journal of Organic Chemistry
Volume

61

Issue

2

Start page

771

End page

4

Subjects

Substitution reaction (arom.

•

intramol.

•

prepn of cycloisodityrosine atropisomers via an intramol. nucleophilic arom. substitution reaction)

•

intramol nucleophilic arom substitution tyrosylfluoronitrophenylalanine; cycloisodityrosine prepn

Note

CAN 124:176902

34-3

Amino Acids, Peptides, and Proteins

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

Journal

written in English.

173912-65-7P Role: BYP (Byproduct), PREP (Preparation) (prepn of cycloisodityrosine atropisomers via an intramol. nucleophilic arom. substitution reaction); 64755-14-2DP (Bouvardin); 83858-82-6DP (Piperazinomycin) Role: PNU (Preparation, unclassified), PREP (Preparation) (prepn of cycloisodityrosine atropisomers via an intramol. nucleophilic arom. substitution reaction); 3978-80-1; 36394-75-9; 109838-85-9; 131858-37-2 Role: RCT (Reactant), RACT (Reactant or reagent) (prepn of cycloisodityrosine atropisomers via an intramol. nucleophilic arom. substitution reaction); 160247-84-7P; 160247-85-8P; 160247-86-9P; 173912-66-8P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn of cycloisodityrosine atropisomers via an intramol. nucleophilic arom. substitution reaction); 173912-67-9P; 174060-77-6P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn of cycloisodityrosine atropisomers via an intramol. nucleophilic arom. substitution reaction)

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/20.500.14299/58562
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