A Novel Ru(VII)/Ru(IV) Mediatory System for Electrooxidation of Primary and Secondary Alcohols, Leading to Aldehydes and Ketones

1995 ◽  
Vol 24 (5) ◽  
pp. 369-370 ◽  
Author(s):  
Sigeru Torii ◽  
Akihito Yoshida
2020 ◽  
Vol 17 ◽  
Author(s):  
Majid M. Heravi ◽  
Tayebe Momeni ◽  
Vahideh Zadsirjan ◽  
Leila Mohammadi

: Dess–Martin periodinane (DMP), is a commercially available chemical, frequently being utilized as a mild oxidative agent for the selective oxidation of primary and secondary alcohols to their corresponding aldehydes and ketones, respectively. DMP shows several merits over other common oxidative agent such as chromium- and DMSO-based oxidants, thus it is habitually employed in the total synthesis of natural products. In this review, we try to underscore the applications of DMP as an effective oxidant in an appropriate step (steps) in the multistep total synthesis of natural products.


2020 ◽  
Vol 22 (2) ◽  
pp. 471-477 ◽  
Author(s):  
Nikolaos F. Nikitas ◽  
Dimitrios Ioannis Tzaras ◽  
Ierasia Triandafillidi ◽  
Christoforos G. Kokotos

A mild and green photochemical protocol for the oxidation of alcohols to aldehydes and ketones was developed.


Author(s):  
Andrew Bogdan ◽  
D Tyler McQuade

We demonstrate the preparation and characterization of a simplified packed-bed microreactor using an immobilized TEMPO catalyst shown to oxidize primary and secondary alcohols via the biphasic Anelli-Montanari protocol. Oxidations occurred in high yields with great stability over time. We observed that plugs of aqueous oxidant and organic alcohol entered the reactor as plugs but merged into an emulsion on the packed-bed. The emulsion coalesced into larger plugs upon exiting the reactor, leaving the organic product separate from the aqueous by-products. Furthermore, the microreactor oxidized a wide range of alcohols and remained active in excess of 100 trials without showing any loss of catalytic activity.


1969 ◽  
Vol 47 (19) ◽  
pp. 3705-3707 ◽  
Author(s):  
D. V. Ramana ◽  
C. N. Pillai

Alumina containing about 2.2% by weight of Na+ has been found to be an effective catalyst for the vapor phase reduction of carbonyl compounds by alcohols and for the reverse reaction, the oxidation of the alcohols by carbonyl compounds. The reduction of a number of aliphatic and aromatic aldehydes and ketones by isopropyl alcohol and the oxidation of a number of primary and secondary alcohols by ketones like acetone and cyclohexanone are reported.


2020 ◽  
Author(s):  
John A Lepore ◽  
David Keeley ◽  
Eliza Merges ◽  
Jasmine Uralil ◽  
Katelynn Dux ◽  
...  

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