Cationic cyclization reactions with alkyne terminating groups: a useful tool in biomimetic synthesis

2022 ◽  
Author(s):  
Olaya García-Pedrero ◽  
Félix Rodríguez

Cyclization reactions through cationic intermediates have become a highly valuable tool in organic synthesis. The use of alkynes as the terminating group in this type of cationic processes offers wide...

2021 ◽  
Vol 25 ◽  
Author(s):  
Saima malik ◽  
Aditya G. Lavekar ◽  
Bimal Krishna Banik

: The radical was first come into existence in 1900 by Gomberg, where the triphenylmethane radical was explored. Thus, even to date, two centuries have seen radical chemistry as the methodology of preference in organic synthesis. Due to the fascinating nature of the radical-mediated cyclization reactions, it always caught the eye of organic chemists for the synthesis of novel organic compounds with diverse stereochemistry. Moreover, the development of radical methods further proves beneficial for the synthesis by providing atom- and step-economical methods to complex molecules. Among these, where radical chemistry has been employed, the use of tin-based radical annulation is the most common and widely used field for the synthesis of a wide range of organic reactions with medicinal importance. In this review, we compiled recent tin-mediated radical cyclization reactions toward the synthesis of molecules of biological significance.


2017 ◽  
Vol 41 (16) ◽  
pp. 7824-7835 ◽  
Author(s):  
Mukhtiar Ahmed ◽  
Muhammad Moazzam Naseer

Cyclization reactions are considered as one of the most important reactions in organic synthesis due to the fact that natural molecules contain cyclic components either as part of the molecule or molecular skeleton.


ChemInform ◽  
2004 ◽  
Vol 35 (51) ◽  
Author(s):  
Peter Langer ◽  
Walter Freiberg

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