New and Efficient Synthesis of Oligomeric PorphyrinsviaStepwise Nucleophilic Substitution of Aminoporphyrins to Cyanuric Chloride

1995 ◽  
Vol 24 (8) ◽  
pp. 631-632 ◽  
Author(s):  
Kanako Ichihara ◽  
Yoshinori Naruta
2019 ◽  
Vol 43 (1-2) ◽  
pp. 14-19
Author(s):  
Shuting Li ◽  
Wanfeng Yang ◽  
Min Ji ◽  
Jin Cai ◽  
Junqing Chen

A new and efficient synthesis of 6-bromo-8-cyclopentyl-5-methyl-2-(methylsulfinyl)-pyrido[2,3-d]pyrimidin-7(8H)-one, a key intermediate of Palbociclib, starting from thiouracil was described. This protocol involved methylation, nucleophilic substitution, bromination, nucleophilic substitution, Heck reaction, ring closure, oxidation, and bromination to afford a key intermediate of Palbociclib with approximately 35% overall yield. The advantages of this developed synthetic strategy included improved overall yield, inexpensive starting materials, and readily controllable and cleaner reaction conditions.


Synlett ◽  
2017 ◽  
Vol 29 (04) ◽  
pp. 525-529 ◽  
Author(s):  
Sigitas Tumkevicius ◽  
Jonas Bucevicius ◽  
Maris Turks

A simple and efficient synthesis of isomeric 7-deazapurine–1,2,3-triazole conjugates with amino substituents from readily available 9-alkyl-2,6-diazido-7-deazapurines has been developed using consecutive CuAAC and regioselective nucleophilic substitution reactions of ­azido and 1,2,3-triazole groups with amines.


2007 ◽  
Vol 8 (11) ◽  
pp. 1595-1598 ◽  
Author(s):  
Mohammad A. Bigdeli ◽  
Majid M. Heravi ◽  
Gholam Hossein Mahdavinia

Author(s):  
Panagiota Bika ◽  
Vitaly Osokin ◽  
Tatiana Giannakopoulou ◽  
Nadia Todorova ◽  
Mo Li ◽  
...  

Covalent triazine frameworks (CTFs) synthesized through nucleophilic substitution of 4,4’ bipyridine on the carbon atoms of cyanuric chloride were studied as fluorescent sensors. The band gap of the materials was...


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