Micelle-mediated organic synthesis: the synthesis and characterization of three new polycyclic dioxa cage compounds

1984 ◽  
Vol 49 (7) ◽  
pp. 1295-1297 ◽  
Author(s):  
James K. Sutter ◽  
Chaim N. Sukenik
Synthesis ◽  
2018 ◽  
Vol 50 (09) ◽  
pp. 1737-1749 ◽  
Author(s):  
Tetsuaki Fujihara ◽  
Yasushi Tsuji

Herein, copper-catalyzed borylative and silylative transformations of allenes using borylcopper or silylcopper as the active catalytic species are described. First, the synthesis and characterization of borylcopper and silylcopper complexes are briefly introduced. Next, the borylative transformations of allenes are summarized including hydro­boration, carboboration, and borylative allylation of carbonyl compounds. We next deal with the silylative transformations of allenes such as hydrosilylation, carbosilylation, and silylative allylation of carbonyl compounds.1 Introduction2 Synthesis of Borylcopper and Silylcopper Complexes3 Borylative Transformations4 Silylative Transformations5 Conclusions and Future Outlook


2017 ◽  
Vol 59 (3) ◽  
pp. 300-307
Author(s):  
Shashi Kala Devi ◽  
Jyoti Malviya ◽  
L. K. Sharma ◽  
R. K. P. Singh

2008 ◽  
Vol 56 (6) ◽  
pp. 749-752
Author(s):  
Abdolmajid Bayandori Moghaddam ◽  
Mohammad Reza Ganjali ◽  
Rassoul Dinarvand ◽  
Maryam Latifi ◽  
Parviz Norouzi

2011 ◽  
Vol 5 (1) ◽  
pp. 37-40 ◽  
Author(s):  
Vasant Chabukswar ◽  
◽  
Sanjay Bhavsar ◽  
Amit Horne ◽  
◽  
...  

2015 ◽  
Vol 2015 ◽  
pp. 1-8
Author(s):  
Álvaro Fontana ◽  
Fábio Santana dos Santos ◽  
Flávia Aparecida Fonseca ◽  
Adonilson Dos Reis Freitas ◽  
Andersson Barison ◽  
...  

Organic synthesis of the monomer of poly(p-phenylenevinylene) was performed starting by the 2,5-dimethylphenol compound. An iodine atom was added to one end of the aromatic ring and then the iodine atom was substituted by a cyano group. Opposite to the cyano group was added a chain of six carbon atoms and the end of the carbon chain has an added bromine atom. The characterizations of the obtained compounds were made by FTIR, GC-MS,1H, and13C NMR and showed that almost all of the proposed monomers were obtained in their totality.


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