Reagents for organic synthesis. 5. Synthesis of aldehydes and ketones from nitro paraffins

1985 ◽  
Vol 50 (24) ◽  
pp. 4971-4973 ◽  
Author(s):  
Kosta Steliou ◽  
Marc Andre Poupart
Author(s):  
Alan R. Katritzky ◽  
Michael J. Cook ◽  
S. Bruce Brown ◽  
Raymundo Cruz ◽  
George H. Millet ◽  
...  

1996 ◽  
Vol 61 (12) ◽  
pp. 1697-1702 ◽  
Author(s):  
Josef Vágner ◽  
Viktor Krchňák ◽  
Michal Lebl ◽  
George Barany

Phosphorane ylides and phosphonate anions react smoothly with resin-bound aldehydes and ketones to provide alkenes in good yields and purities (assessed after cleavage of acid-labile PAL anchor to support). The reactions of aldehydes give excellent stereoselectivities. Effective conditions have been developed for carrying out these transformations.


1980 ◽  
Vol 11 (5) ◽  
Author(s):  
A. R. KATRITZKY ◽  
M. J. COOK ◽  
S. B. BROWN ◽  
R. CRUZ ◽  
G. H. MILLET ◽  
...  

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Dawei Cao ◽  
Chen-Chen Li ◽  
Huiying Zeng ◽  
Yong Peng ◽  
Chao-Jun Li

AbstractAldehydes and ketones are widely found in biomass resources and play important roles in organic synthesis. However, the direct deoxygenative coupling of aldehydes or ketones to construct C(sp3)−C(sp3) bond remains a scientific challenge. Here we report a nickel−catalyzed reductive homo-coupling of moisture- and air-stable hydrazones generated in-situ from naturally abundant aldehydes and ketones to construct challenging C(sp3)−C(sp3) bond. This transformation has great functional group compatibility and can suit a broad substrate scope with innocuous H2O, N2 and H2 as the by-products. Furthermore, the application in several biological molecules and the transformation of PEEK model demonstrate the generality, practicability, and applicability of this novel methodology.


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