Photochemical reactions in organic synthesis: A novel and efficient route to angular and linear tetraquinanes

Tetrahedron ◽  
1996 ◽  
Vol 52 (45) ◽  
pp. 14287-14296 ◽  
Author(s):  
Vishwakarma Singh ◽  
Prathap .S
2021 ◽  
Vol 18 ◽  
Author(s):  
Aparna Das

: In recent years, photocatalytic technology has shown great potential as a low-cost, environmentally friendly, and sustainable technology. Compared to other light sources in photochemical reaction, LEDs have advantages in terms of efficiency, power, compatibility, and environmentally-friendly nature. This review highlights the most recent advances in LED-induced photochemical reactions. The effect of white and blue LEDs in reactions such as oxidation, reduction, cycloaddition, isomerization, and sensitization is discussed in detail. No other reviews have been published on the importance of white and blue LED sources in the photocatalysis of organic compounds. Considering all the facts, this review is highly significant and timely.


Author(s):  
Yeshua Sempere ◽  
Martin Morgenstern ◽  
Thorsten Bach ◽  
Manuel Plaza

AbstractIn recent years, photochemical reactions have emerged as powerful transformations which significantly expand the repertoire of organic synthesis. However, a certain lack of selectivity can hamper their application and limit their scope. In this context, a major research effort continues to focus on an improved control over stereo- and chemoselectivity that can be achieved in molecular assemblies between photosubstrates and an appropriate host molecule. In this tutorial review, some recent, representative examples of photochemical reactions have been collected whose unique outcome is dictated by the formation of a molecular assembly driven by non-covalent weak interactions. Graphical Abstract


2000 ◽  
Vol 72 (7) ◽  
pp. 1321-1326 ◽  
Author(s):  
Angelo Albini ◽  
Maurizio Fagnoni ◽  
Mariella Mella

Photochemical reactions are expected to have an increasing role in organic synthesis with the drive towards environment-friendly reactions. Some examples illustrating the scope and versatility of radical alkylation of electrophilic alkenes via photoinduced electron transfer are presented. A few applications in special fields are mentioned.


Organics ◽  
2021 ◽  
Vol 2 (3) ◽  
pp. 287-305
Author(s):  
Matthieu Pélingre ◽  
Dindet Steve-Evanes Koffi Teki ◽  
Jamal El-Abid ◽  
Vincent Chagnault ◽  
José Kovensky ◽  
...  

Many preparations of maltooligosaccharides have been described in literature, essentially using enzymatic or biotechnological processes. These compounds, derived from starch, are well-known as prebiotic agents. The use of maltohexa-, hepta-, and octaoses as synthons in organic synthesis was also well documented in literature. They can indeed be obtained as single compounds by the cyclodextrins’ ring-opening. This reaction has been studied for many years, varying the protecting and functional groups and the reaction conditions, leading to functionalized oligomaltoses. These compounds are of wide interest in various fields. They have a strong potential as scaffolds for multivalence in chemobiology, as building blocks for the production of biomimetic pseudo-glycopeptides, as well as monomers for the preparation of materials. In view of the importance of these oligomaltoses, this review focuses on the different methodologies allowing access to them via chemical and enzymatic ring-opening of cyclodextrins.


2008 ◽  
Vol 108 (3) ◽  
pp. 1052-1103 ◽  
Author(s):  
Norbert Hoffmann

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