scholarly journals Synthesis of γ-substituted carbonyl compounds from DMSO-mediated oxidation of enynamides: mechanistic insights and carbon- and hetero-functionalizations

2019 ◽  
Vol 10 (38) ◽  
pp. 8799-8805 ◽  
Author(s):  
Quynh H. Nguyen ◽  
Nguyen H. Nguyen ◽  
Hanbyul Kim ◽  
Seunghoon Shin

1,3-Enynamides underwent oxygenative coupling with carbon- and heteroatom nucleophiles with high remote selectivity. Kinetic analysis revealed a continuum mechanism between concerted SN2′′ and via a carbocation, depending on the nucleophiles used.

1991 ◽  
Vol 32 (8) ◽  
pp. 1007-1010 ◽  
Author(s):  
Pramod K. Arora ◽  
Lawrence M. Sayre

2013 ◽  
Vol 9 ◽  
pp. 1437-1442 ◽  
Author(s):  
Nida Ambreen ◽  
Ravi Kumar ◽  
Thomas Wirth

Hypervalent iodine(III)/TEMPO-mediated oxidation of various aliphatic, aromatic and allylic alcohols to their corresponding carbonyl compounds was successfully achieved by using microreactor technology. This method can be used as an alternative for the oxidation of various alcohols achieving excellent yields and selectivities in significantly shortened reaction times.


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

RSC Advances ◽  
2018 ◽  
Vol 8 (56) ◽  
pp. 32055-32062 ◽  
Author(s):  
Ajay H. Bansode ◽  
Gurunath Suryavanshi

A highly efficient, metal free rapid protocol studied mechanistically the oxidation of primary and secondary amines to their corresponding carbonyl compounds using PhI(OAc)2and catalytic TEMPO to provide diverse products in excellent yields.


Molecules ◽  
2008 ◽  
Vol 13 (6) ◽  
pp. 1230-1237 ◽  
Author(s):  
Francesco Ballistreri ◽  
Ugo Chiacchio ◽  
Antonio Rescifina ◽  
Gaetano Tomaselli ◽  
Rosa Toscano

RSC Advances ◽  
2015 ◽  
Vol 5 (23) ◽  
pp. 17383-17388 ◽  
Author(s):  
Wei Liu ◽  
Sheng Liu ◽  
Hongqi Xie ◽  
Zhixing Qing ◽  
Jianguo Zeng ◽  
...  

Visible light promoted the oxidation of compounds 1 to amides 2 which were easily transferred to compounds 12.


2016 ◽  
Vol 473 (6) ◽  
pp. 717-731 ◽  
Author(s):  
Pierre-Alexandre Lallement ◽  
Thomas Roret ◽  
Pascale Tsan ◽  
José M. Gualberto ◽  
Jean-Michel Girardet ◽  
...  

The resolution of a NMR structure of a poplar dehydroascorbate reductase (DHAR) coupled to kinetic analysis and GSSG-mediated oxidation treatments revealed that DHARs are highly specialized for dehydroascorbate reduction and adopt different redox states depending on the number of cysteine residues.


ChemInform ◽  
2010 ◽  
Vol 22 (51) ◽  
pp. no-no
Author(s):  
P. K. ARORA ◽  
L. M. SAYRE

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