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Facile oxidation of flavanones to flavones using [hydroxy(tosyloxy)iodo]benzene in an ionic liquid

Murugan Muthukrishnan 1
Murugan Muthukrishnan
, 
Pratap S Patil 1
Pratap S Patil
, 
Shivaji V More 1
Shivaji V More
, 
Ramesh A Joshi 1
Ramesh A Joshi
10.1070/MC2005v015n03ABEH001997
Published 2005-05-04
Communication , Volume 15, Issue 3, 100-101
16
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Muthukrishnan M. et al. Facile oxidation of flavanones to flavones using [hydroxy(tosyloxy)iodo]benzene in an ionic liquid // Mendeleev Communications. 2005. Vol. 15. No. 3. pp. 100-101.
GOST all authors (up to 50) Copy
Muthukrishnan M., Patil P. S., More S. V., Joshi R. A. Facile oxidation of flavanones to flavones using [hydroxy(tosyloxy)iodo]benzene in an ionic liquid // Mendeleev Communications. 2005. Vol. 15. No. 3. pp. 100-101.
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TY - JOUR
DO - 10.1070/MC2005v015n03ABEH001997
UR - https://mendcomm.colab.ws/publications/10.1070/MC2005v015n03ABEH001997
TI - Facile oxidation of flavanones to flavones using [hydroxy(tosyloxy)iodo]benzene in an ionic liquid
T2 - Mendeleev Communications
AU - Muthukrishnan, Murugan
AU - Patil, Pratap S
AU - More, Shivaji V
AU - Joshi, Ramesh A
PY - 2005
DA - 2005/05/04
PB - Mendeleev Communications
SP - 100-101
IS - 3
VL - 15
ER -
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@article{2005_Muthukrishnan,
author = {Murugan Muthukrishnan and Pratap S Patil and Shivaji V More and Ramesh A Joshi},
title = {Facile oxidation of flavanones to flavones using [hydroxy(tosyloxy)iodo]benzene in an ionic liquid},
journal = {Mendeleev Communications},
year = {2005},
volume = {15},
publisher = {Mendeleev Communications},
month = {May},
url = {https://mendcomm.colab.ws/publications/10.1070/MC2005v015n03ABEH001997},
number = {3},
pages = {100--101},
doi = {10.1070/MC2005v015n03ABEH001997}
}
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Muthukrishnan, Murugan, et al. “Facile oxidation of flavanones to flavones using [hydroxy(tosyloxy)iodo]benzene in an ionic liquid.” Mendeleev Communications, vol. 15, no. 3, May. 2005, pp. 100-101. https://mendcomm.colab.ws/publications/10.1070/MC2005v015n03ABEH001997.

Abstract

A method for the oxidation of flavanones to flavones has been developed using [hydroxy(tosyloxy)iodo]benzene (HTIB) in the room-temperature ionic liquid 1,3-di-n-butylimidazolium bromide ([bbim]+Br–).

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