Palladium-Catalyzed C—O Bond-Forming Reactions

Author(s):  
V. Milata ◽  
S. Rádl ◽  
S. Voltrová
ChemInform ◽  
2012 ◽  
Vol 43 (27) ◽  
pp. no-no
Author(s):  
Satoshi Ueda ◽  
Siraj Ali ◽  
Brett P. Fors ◽  
Stephen L. Buchwald

2018 ◽  
Vol 22 (08) ◽  
pp. 619-631 ◽  
Author(s):  
Inna A. Abdulaeva ◽  
Kirill P. Birin ◽  
Yulia G. Gorbunova ◽  
Aslan Yu. Tsivadze ◽  
Alla Bessmertnykh-Lemeune

Several methods for the post-synthetic modification of imidazo[4,5-[Formula: see text]]porphyrins are reported. First, a synthetic approach to the isomeric difunctionalized porphyrins, containing two [Formula: see text]-fused 2-aryl-1[Formula: see text]-imidazole cycles at adjacent or opposite pyrrole rings of the macrocycle is developed. The core chemistry of this synthetic route is the transformation of 2-aryl-1[Formula: see text]-imidazo[4,5-[Formula: see text]]porphyrins into corresponding imidazodioxochlorins followed by Debus–Radziszewski condensation with aromatic aldehyde. Next, 2-(4-bromophenyl)-1[Formula: see text]-imidazo[4,5-[Formula: see text]]-5,10,15,20-tetramesitylporphyrin was transformed into useful carboxy- and phosphonato-substituted precursors for material chemistry according to palladium-catalyzed C–C and C–P bond forming reactions.


2012 ◽  
Vol 77 (5) ◽  
pp. 2543-2547 ◽  
Author(s):  
Satoshi Ueda ◽  
Siraj Ali ◽  
Brett P. Fors ◽  
Stephen L. Buchwald

Synlett ◽  
2011 ◽  
Vol 2011 (12) ◽  
pp. 1766-1768
Author(s):  
Hidemi Yoda ◽  
Tetsuya Sengoku ◽  
Tomoya Hamamatsu ◽  
Toshiyasu Inuzuka ◽  
Masaki Takahashi

2010 ◽  
Vol 8 (20) ◽  
pp. 4518 ◽  
Author(s):  
Roberta Berrino ◽  
Sandro Cacchi ◽  
Giancarlo Fabrizi ◽  
Antonella Goggiamani ◽  
Paolo Stabile

ChemInform ◽  
2014 ◽  
Vol 45 (42) ◽  
pp. no-no
Author(s):  
Krishnan Ramachandiran ◽  
Thonthula Sreelatha ◽  
Neelakandan V. Lakshmi ◽  
Thelagathoti H. Babu ◽  
Doraiswamy Muralidharan ◽  
...  

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