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  4. Synthesis of polycyclic aminal heterocycles via decarboxylative cyclisation of dipeptide derivatives
 
research article

Synthesis of polycyclic aminal heterocycles via decarboxylative cyclisation of dipeptide derivatives

Robert, Emma G. L.
•
Le Du, Eliott  
•
Waser, Jerome  
February 15, 2022
Chemical Communications (ChemComm)

An oxidative-decarboxylative intramolecular cyclisation of dipeptide derivatives is reported. This transformation is promoted by phenyl iodine(iii) diacetate (PIDA) in combination with BF3 center dot OEt2. The reaction gives access to a variety of valuable polycyclic N-heterocyclic scaffolds containing 5-, 6-, or 7-membered rings.

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Type
research article
DOI
10.1039/d2cc00167e
Web of Science ID

WOS:000760162100001

Author(s)
Robert, Emma G. L.
Le Du, Eliott  
Waser, Jerome  
Date Issued

2022-02-15

Publisher

Royal Society of Chemistry

Published in
Chemical Communications (ChemComm)
Volume

58

Issue

21

Start page

3473

End page

3476

Subjects

Chemistry, Multidisciplinary

•

Chemistry

•

n-acyliminium ions

•

acids

•

alkaloids

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LCSO  
FunderGrant Number

FNS

200020_182798)

RelationURL/DOI

IsSupplementedBy

https://doi.org/10.5281/zenodo.5940081
Available on Infoscience
March 14, 2022
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/186253
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