Palladium-Catalyzed Cleavage of P-C Bonds in Quaternary Phosphonium Salts and Its Applications to Organic Synthesis

1995 ◽  
Vol 24 (12) ◽  
pp. 1101-1102 ◽  
Author(s):  
Masato Sakamoto ◽  
Isao Shimizu ◽  
Akio Yamamoto
Keyword(s):  
Organic Synthesis ◽  
Phosphonium Salts ◽  
Palladium Catalyzed ◽  
Quaternary Phosphonium Salts

The Study of the Conformation and Dynamics of the New Quaternary Phosphonium Salts by NMR Spectroscopy

2014 ◽  
Vol 45 (7) ◽  
pp. 653-665 ◽  
Author(s):  
Oksana Aganova ◽  
Leisan Galiullina ◽  
Albert Aganov ◽  
Yurii Shtyrlin ◽  
Mikhail Pugachev ◽  
...  
Keyword(s):  
Nmr Spectroscopy ◽  
Phosphonium Salts ◽  
Quaternary Phosphonium Salts

Orthogonal Investigation of Influencing Factors on the Modification of Montmorillonite by THPC in Acid Conditions

2014 ◽  
Vol 936 ◽  
pp. 1017-1021
Author(s):  
Pan Chen ◽  
Jin Cheng Wang
Keyword(s):  
Reaction Time ◽  
Ion Exchange ◽  
Influencing Factors ◽  
Reaction Temperature ◽  
Orthogonal Test ◽  
Test Results ◽  
Phosphonium Salts ◽  
Exchange Reactions ◽  
Quaternary Phosphonium Salts

Na-MMT was modified with quaternary phosphonium salts, tetramethylolphosphonium chloride (THPC), via ion-exchange reactions, in acid conditions. Different factors such as reaction time , reaction temperature, the types of solvent, and CEC ratios, were investigated using orthogonal test. Results showed that the best combination of these four factors were A1B3C1D1, that is, the type of the solvent was acetone and water (1:1), reaction time was 3h, CEC ratio was 1:1, and the reaction temperature was 80°C.

scholarly journals Palladium-Catalyzed Coupling Reactions on Functionalized 2-Trifluoromethyl-4-chromenone Scaffolds: Synthesis of Highly Functionalized Trifluoromethyl Heterocycles

Synthesis ◽  
2018 ◽  
Vol 51 (06) ◽  
pp. 1342-1352 ◽  
Author(s):  
Javier Izquierdo ◽  
Atul Jain ◽  
Sarki Abdulkadir ◽  
Gary Schiltz
Keyword(s):  
Natural Products ◽  
Organic Synthesis ◽  
Biological Activities ◽  
Structural Complexity ◽  
Biologically Active ◽  
Coupling Reactions ◽  
Trifluoromethyl Group ◽  
Palladium Catalyzed ◽  
Active Natural

The chromenone core is an ubiquitous group in biologically active natural products and has been extensively used in organic synthesis. Fluorine-derived compounds, including those with a trifluoromethyl group (CF3), have shown enhanced biological activities in numerous pharmaceuticals compared with their non-fluorinated analogues. 2-Trifluoromethylchromenones can be readily functionalized at the 8- and 7-positions, providing chromenones cores of high structural complexity, which are excellent precursors for numerous trifluoromethyl heterocycles.

Peri-Interactions in Naphthalenes, 9 [1]. On Hypercoordination in Non-Quaternary Phosphonium Salts and a Secondary Phosphine with the (8-Dimethylamino-Naphth-1-Yl) Substituent

2003 ◽  
Vol 58 (1) ◽  
pp. 59-73 ◽  
Author(s):  
Günter Paulus Schiemenz ◽  
Christian Näther ◽  
Simon Pörksen
Keyword(s):  
Hydrogen Bonds ◽  
Basic Assumption ◽  
Coupling Constants ◽  
Secondary Phosphine ◽  
Phosphonium Salts ◽  
Silicon Compounds ◽  
Nmr Data ◽  
Yield Information ◽  
Quaternary Phosphonium Salts

Abstract The 31P NMR data of non-quaternary (8-dimethylamino-naphth-1-yl)phosphonium salts, with emphasis on the 1J(31P, 1H) coupling constants, where scrutinized for their potential to yield information about N→P dative interactions. As for δ (29Si) and 1J(29Si, 1H) in the isosteric silanes, the data do not permit conclusions in favour of such interactions. 1J(31P, 1H) of bis(8-dimethylaminonaphth- 1-yl)phosphine in conjunction with the distances d(N···P) invalidates the basic assumption on which the claim of dative N→P/Si bonding in such phosphorus and silicon compounds rests, viz. that N···P/Si distances of ca. 270 pm are evidence for P/Si-hypercoordination. No evidence for hydrogen bonds N···H-P was found.

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