Recent advances in catalyst-free photochemical reactions via electron-donor-acceptor (EDA) complex process

2020 ◽  
Vol 61 (8) ◽  
pp. 151506 ◽  
Author(s):  
Yan-qin Yuan ◽  
Swarup Majumder ◽  
Ming-hua Yang ◽  
Sheng-rong Guo
2020 ◽  
Author(s):  
José Tiago Menezes Correia ◽  
Gustavo Piva da Silva ◽  
Camila Menezes Kisukuri ◽  
Elias André ◽  
Bruno Pires ◽  
...  

A metal- and catalyst-free photoinduced radical cascade hydroalkylation of 1,7-enynes has been disclosed. The process is triggered by a SET event involving a photoexcited electron-donor-aceptor complex between NHPI ester and Hantzsch ester, which decomposes to afford a tertiary radical that is readily trapped by the enyne. <a>The method provides an operationally simple, robust and step-economical approach to the construction of diversely functionalized dihydroquinolinones bearing quaternary-centers. A sequential one-pot hydroalkylation-isomerization approach is also allowed giving access to a family of quinolinones. A wide substrate scope and high functional group tolerance was observed in both approaches</a>.


2021 ◽  
Vol 243 ◽  
pp. 109734
Author(s):  
Audrey Gilbert ◽  
Mélodie Birepinte ◽  
Jean-François Paquin

2002 ◽  
Vol 06 (04) ◽  
pp. 289-295 ◽  
Author(s):  
Dirk M. Guldi ◽  
Shunichi Fukuzumi

Recent advances in electron transfer chemistry of electron donor-acceptor ensembles reported containing porphyrins and metalloporphyrins reported in ICPP-2 are reviewed briefly by focusing on the fundamental aspects of electron transfer reactions.


2019 ◽  
Vol 23 (3) ◽  
pp. 276-312 ◽  
Author(s):  
Purushothaman Gopinath ◽  
Srinivasan Chandrasekaran

Diactivated cyclopropanes containing two geminal electron withdrawing groups, commonly called as ‘Doubly Activated Cyclopropanes’ are useful synthons for the synthesis of many interesting natural products and functionalized molecules. These geminal electron withdrawing groups (EWG’s) facilitate the regioselective ring opening of cyclopropanes by polarizing the C-C bond adjacent to it. This polarization also allows them to undergo 1,3 dipolar cycloaddition reactions when substituted with a suitable electron donor substituent at the adjacent carbon (donor-acceptor cyclopropanes) in the presence of suitable dipolarophiles. In this review, we discuss the recent advances in the chemistry of doubly activated cyclopropanes: their synthesis, reactions and applications in total synthesis.


2004 ◽  
Vol 08 (07) ◽  
pp. 976-983 ◽  
Author(s):  
Dirk M. Guldi ◽  
Hiroshi Imahori

Recent advances in electron transfer chemistry of supramolecular electron donor-acceptor assemblies – containing porphyrins and metalloporphyrins – in connection with ICPP-3 are reviewed briefly by focusing on aspects of electron and energy transfer reactions.


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