pyridinium chlorochromate

Author(s):  
B. Cornils
1999 ◽  
Vol 23 (2) ◽  
pp. 118-119
Author(s):  
Vaishali Chakraborty ◽  
Manobjyoti Bordoloi

An efficient and mild methodology for the oxidation of alcohols to the corresponding carbonyl functions is described using pyridinium chlorochromate under microwave irradiation.


Synthesis ◽  
1978 ◽  
Vol 1978 (03) ◽  
pp. 212-213 ◽  
Author(s):  
John R. MALONEY ◽  
Robert E. LYLE ◽  
Jose E SAAVEDRA ◽  
Gloria G. LYLE

1997 ◽  
Vol 274 (1-3) ◽  
pp. 106-111 ◽  
Author(s):  
Z. Paja̧k ◽  
B. Szafrańska ◽  
P. Czarnecki ◽  
J. Mayer ◽  
A. Kozak

Synthesis ◽  
1980 ◽  
Vol 1980 (03) ◽  
pp. 223-224 ◽  
Author(s):  
Yu-Shia Cheng ◽  
Wen-Liang Liu ◽  
Shu-hsia Chen

Synthesis ◽  
1984 ◽  
Vol 1984 (03) ◽  
pp. 280-281 ◽  
Author(s):  
R. Antonioletti ◽  
M. D'Auria ◽  
A. De Mico ◽  
G. Piancatelli ◽  
A. Scettri

Molecules ◽  
2022 ◽  
Vol 27 (2) ◽  
pp. 548
Author(s):  
Bernard L. Adjei ◽  
Frederick A. Luzzio

A systematic study of the oxidation of 3-hydroxy-2-substituted isoindolin-1-ones (hydroxylactams) and their conversion to the corresponding phthalimides was undertaken using three oxidants. Of special interest was the introduction of nickel peroxide (NiO2) as an oxidation system for hydroxylactams and comparison of its performance with the commonly used pyridinium chlorochromate (PCC) and iodoxybenzoic acid (IBX) reagents. Using a range of hydroxylactams, optimal conversions of these substrates to the corresponding imides was achieved with 50 equivalents of freshly prepared NiO2 in refluxing toluene over 5–32 h reaction times. By comparison, oxidations of the same substrates using PCC/silica gel (three equivalents) and IBX (three equivalents) required oxidation times of 1–3 h for full conversion but required lengthier purification. While nominal amounts (~25 mg) of substrate hydroxylactams were used to ascertain conversion, scale-up procedures using all three methods gave good to excellent isolated yields of imides.


2010 ◽  
Vol 8 (1) ◽  
pp. 91-93
Author(s):  
Hanoch J. Sohilait

In these studies, Pyridinium chlorochromate-Alumina was used for oxidation of secondary alcohols (safryl alcohol and methyleugenyl alcohol) to ketone.  The oxidation of safryl alcohol with PCC-Al2O3 followed by purification by potassium bisulfite yields safryl ketone (62,92%). The oxidation of methyleugenyl alcohol with PCC-Al2O3, followed by purification by potassium bisulfite  yields methyleugenyl ketone (68,04%). The elucidation of these products was analyzed by FTIR, 1H-NMR and MS.   Keywords : PCC-alumina, secondary alcohols, ketone


1978 ◽  
Vol 43 (13) ◽  
pp. 2618-2621 ◽  
Author(s):  
Jean M. J. Frechet ◽  
James Warnock ◽  
M. Jean Farrall

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