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  4. SNAr-Based Macrocyclization: An Application to the Synthesis of Vancomycin Family Models
 
research article

SNAr-Based Macrocyclization: An Application to the Synthesis of Vancomycin Family Models

Beugelmans, Rene
•
Singh, Girij Pal
•
Bois-Choussy, Michele
Show more
1994
The Journal of Organic Chemistry

The first examples of macrocyclization using the intramol. SNAr reaction are reported. The method has allowed the efficient prepn. of the elusive 16-membered macrocyclic COD and DOE rings related to vancomycin. The mild conditions used allow the incorporation of very racemization-prone amino acids, such as p-methoxyphenylglycine, into the peptide chain. After serving as an activator, the nitro group ortho to the diaryl ether linkage is converted either into a chlorine or a hydrogen atom, thus achieving the substitution pattern found in the vancomycin family of glycopeptides. When compd. I 20 was submitted to the same macrocyclization conditions, two atropisomers II 21 and III 22 were isolated and characterized. [on SciFinder (R)]

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Type
research article
DOI
10.1021/jo00098a010
Author(s)
Beugelmans, Rene
Singh, Girij Pal
Bois-Choussy, Michele
Chastanet, Jacqueline
Zhu, Jieping  
Date Issued

1994

Published in
The Journal of Organic Chemistry
Volume

59

Issue

19

Start page

5535

End page

42

Subjects

Ring closure and formation (macrocyclization

•

SNAr-based

•

in synthesis of COD and DOE rings of vancomycin)

•

SNAr macrocyclization COD DOE ring vancomycin

Note

CAN 122:133774

34-3

Amino Acids, Peptides, and Proteins

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

Journal

written in English.

621-37-4 Role: RCT (Reactant), RACT (Reactant or reagent) (acylation by, of glycine fluoronitrophenylethylamide); 13269-15-3 (3-Hydroxybenzylamine hydrochloride) Role: RCT (Reactant), RACT (Reactant or reagent) (amidation by, of protected amino acids); 27460-85-1 Role: RCT (Reactant), RACT (Reactant or reagent) (amidation of, with (fluoronitro)penetylamine); 4530-20-5 (Boc-glycine) Role: RCT (Reactant), RACT (Reactant or reagent) (amidation of, with (fluoronitro)phenetylamine); 15761-38-3 Role: RCT (Reactant), RACT (Reactant or reagent) (amidation of, with hydroxybenzylamine); 160877-33-8P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and O-methylation of); 160877-40-7P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and coupling of, with amino acid hydroxybenzylamides); 157662-78-7P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and coupling of, with glycine deriv.); 160877-34-9P; 160877-45-2P; 160877-46-3P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and deamination of); 157662-75-4P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and diazotization-chlorination of); 160877-38-3P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and hydrolysis of); 157662-71-0P; 157662-72-1P; 160877-41-8P; 160877-42-9P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and macrocyclization of); 157662-73-2P; 157662-74-3P; 157662-77-6P; 157750-78-2P; 160877-43-0P; 160877-44-1P Role: RCT (Reactant), SPN (Synthetic preparation), PREP (Preparation), RACT (Reactant or reagent) (prepn. and redn. of); 147949-76-6P; 160877-39-4P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. and sequential deblocking and coupling of, with (fluoronitrophenyl)propionic acid); 157662-69-6P; 157662-70-9P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. and sequential deblocking and coupling of, with hydroxyphenylacetic acid); 147949-74-4P; 147949-75-5P; 147949-89-1P; 157662-76-5P; 160877-35-0P; 160877-36-1P; 160877-37-2P Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of); 1404-90-6P (Vancomycin) Role: SPN (Synthetic preparation), PREP (Preparation) (prepn. of COD and DOE rings of, via SNAr-based macrocyclization); 15017-52-4 Role: RCT (Reactant), RACT (Reactant or reagent) (reaction of, with cyanide); 105-53-3 (Diethyl malonate) Role: RCT (Reactant), RACT (Reactant or reagent) (reaction of, with fluoronitrobenzyl bromide)

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/20.500.14299/58571
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