Ruthenium(II)-catalyzed C–H activation and (4+2) annulation of aromatic hydroxamic acid esters with allylic amides

2021 ◽  
Author(s):  
Chandan Kumar Giri ◽  
Suman Dana ◽  
Mahiuddin Baidya

A (4+2) annulation under Ru(II)-catalysis is reported using aromatic hydroxamic acid esters as oxidizing directing group and allylic amides as unactivated olefin coupling partners, delivering a wide variety of aminomethyl...

1980 ◽  
Vol 35 (6) ◽  
pp. 727-730
Author(s):  
Oemer Saygin ◽  
Peter Decker

Abstract Nonenzymatic catalysis by bivalent ions of Be, Mg, Ca, Zn, Mn, Ni and Co and bioorganic phosphates of the formation of hydroxamic acids from acetate or amino acids has been studied systematically. Increased yields of hydroxamate were observed at particular combinations of reactants. The most prominent increase (ca. 15-fold) was found with acetate and Ni++, and with a combination of ATP and Be++. Among others especially ribose-5-phosphate and glucose-5-phosphate enhanced yields in the presence of most metal ions. Since no release of inorganic phosphate was observed, this effect cannot be interpreted as an evidence for intermediate transhosphorylation reactions; it may also result from simple catalytic effects of metal sugar complexes.


2015 ◽  
Vol 44 (28) ◽  
pp. 12507-12510 ◽  
Author(s):  
Dawei Gong ◽  
Bowen Hu ◽  
Jing Shi ◽  
Dafa Chen

The reactivities of a trinuclear ruthenium complex with 1,5-hexadiene suggest that the CC double bond is the second directing group in transition-metal catalyzed heteroatom-directed intramolecular C–H/olefin coupling reactions.


Diabetes ◽  
2020 ◽  
Vol 69 (Supplement 1) ◽  
pp. 1832-P
Author(s):  
ANNA SANTORO ◽  
PENG ZHOU ◽  
YAN ZHU ◽  
ODILE D. PERONI ◽  
ANDREW T. NELSON ◽  
...  

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