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  4. The first examples of SNAr-based macrocyclization: synthesis of model carboxylate-binding pockets of vancomycin
 
research article

The first examples of SNAr-based macrocyclization: synthesis of model carboxylate-binding pockets of vancomycin

Beugelmans, Rene
•
Zhu, Jieping  
•
Husson, Nicolas
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1994
Journal of the Chemical Society, Chemical Communications

Model carboxylate-binding pocket C-O-D rings of vancomycin and related glycopeptides were efficiently synthesized by intramol. SNAr reactions. Thus, treatment of precursors I (R = H, 4-HOC6H4) with K2CO3 in DMF gave cyclic diaryl ethers II (R1 = NO2), with II (R = 4-HOC6H4) being a mixt. of atropisomers. II (R = H, R1 = NO2) was further converted into II (R = H, R1 = NH2, H, Cl). [on SciFinder (R)]

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Type
research article
DOI
10.1039/c39940000439
Author(s)
Beugelmans, Rene
Zhu, Jieping  
Husson, Nicolas
Bois-Choussy, Michele
Singh, Girij Pal
Date Issued

1994

Published in
Journal of the Chemical Society, Chemical Communications
Issue

4

Start page

439

End page

40

Subjects

Substitution reaction (arom.

•

intramol.

•

in prepn. of vancomycin C-D ring segment model)

•

intramol nucleophilic arom substitution; vancomycin CD ring segment

Note

CAN 121:180167

34-3

Amino Acids, Peptides, and Proteins

Inst. Chim. Subst. Nat.,CNRS,Gif-sur-Yvette,Fr.

Journal

written in English.

4530-20-5 (N-tert-Butoxycarbonylglycine); 27460-85-1 (N-tert-Butoxycarbonyl-D-(4-hydroxyphenyl)glycine) Role: RCT (Reactant), RACT (Reactant or reagent) (amidation of, with fluoro(nitro)phenethylamine); 621-37-4 (3-Hydroxyphenylacetic acid) Role: RCT (Reactant), RACT (Reactant or reagent) (amidation of, with glycine and arylglycine phenethylamides); 459-57-4 (4-Fluorobenzaldehyde) Role: PROC (Process) (conversion of, into fluoro(nitro)phenylacetonitrile); 157662-78-7P (4-Fluoro-3-nitrophenethylamine) Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and amidation of, with protected amino acids); 157662-72-1P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and intramol. nucleophilic arom. substitution of, atropisomers from); 157662-71-0P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and intramol. nucleophilic arom. substitution of, vancomycin C-D ring segment model from); 157662-73-2P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and redn. of, amino deriv. from); 157662-77-6P (4-Fluoro-3-nitrophenylacetonitrile) Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and selective redn. of, fluoro(nitro)phenethylamine from); 1404-90-6P (Vancomycin) Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of C-D ring segment of, via intramol. nucleophilic arom. substitution); 147949-75-5P; 157662-74-3P; 157662-76-5P; 157750-78-2P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of, via intramol. nucleophilic arom. substitution); 157662-69-6P; 157662-70-9P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn., deblocking, and amidation of, with (hydroxyphenyl)acetic acid); 157662-75-4P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn., diazotization, and redn.or chlorination of)

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/20.500.14299/58570
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