Hypervalent iodine-mediated oxidation of alcohols

2009 ◽  
pp. 2086 ◽  
Author(s):  
Muhammet Uyanik ◽  
Kazuaki Ishihara
1997 ◽  
Vol 62 (20) ◽  
pp. 6974-6977 ◽  
Author(s):  
Antonella De Mico ◽  
Roberto Margarita ◽  
Luca Parlanti ◽  
Andrea Vescovi ◽  
Giovanni Piancatelli

ChemInform ◽  
2009 ◽  
Vol 40 (32) ◽  
Author(s):  
Muhammet Uyanik ◽  
Kazuaki Ishihara

2018 ◽  
Vol 14 ◽  
pp. 1203-1207 ◽  
Author(s):  
Elsa Deruer ◽  
Vincent Hamel ◽  
Samuel Blais ◽  
Sylvain Canesi

An alternative method for forming sulfonates through hypervalent iodine(III) reagent-mediated oxidation of sodium sulfinates has been developed. This transformation involves trapping reactive sulfonium species using alcohols. With additional optimization of the reaction conditions, the method appears extendable to other nucleophiles such as electron-rich aromatic systems or cyclic ethers through a ring opening pathway.


2019 ◽  
Vol 17 (25) ◽  
pp. 6165-6173
Author(s):  
Alessandra Casnati ◽  
Marco Fontana ◽  
Elena Motti ◽  
Nicola Della Ca’

Catalytic synthesis of fluorenols by synchronization of two stoichiometric reactions: (a) Pd(ii)-mediated oxidation of alcohols to ketones and (b) Pd(0)/norbornene-catalyzed reaction of aryl iodides with ortho-bromoacetophenones.


2013 ◽  
Vol 2014 (4) ◽  
pp. 781-787 ◽  
Author(s):  
François Napoly ◽  
Ludivine Jean-Gérard ◽  
Catherine Goux-Henry ◽  
Micheline Draye ◽  
Bruno Andrioletti

Author(s):  
Hirofumi Tohma ◽  
Shinobu Takizawa ◽  
Tomohiro Maegawa ◽  
Yasuyuki Kita

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