Oxidation of meso-Diarylporphyrins by a Hypervalent Iodine Compound: Facile Synthesis of meso-Acyloxyporphyrins and Dioxoporphodimethenes

2014 ◽  
Vol 43 (7) ◽  
pp. 1049-1051 ◽  
Author(s):  
Ken-ichi Yamashita ◽  
Daisuke Hirano ◽  
Motoko S. Asano ◽  
Ken-ichi Sugiura
2004 ◽  
Vol 45 (44) ◽  
pp. 8173-8175 ◽  
Author(s):  
Naokazu Kano ◽  
Masaki Ohashi ◽  
Kazuhisa Hoshiba ◽  
Takayuki Kawashima

2021 ◽  
Author(s):  
Ayham Abazid ◽  
Tom-Niklas Hollwedel ◽  
Boris Nachtsheim

This manuscript describes a highly enantioselective oxidative cyclization of N-Allyl Benzamides and derivatives thereof. This method uses a chiral triazole-based iodine catalyst to generate a hypervalent iodine compound in situ as the active catalytic species. Besides oxazolines, other N-heterocylces such as thiazolines, imidazolines as well as oxanines can be generated in high optical purities. <br>


2015 ◽  
Vol 51 (77) ◽  
pp. 14497-14500 ◽  
Author(s):  
Xuan-Hui Ouyang ◽  
Ren-Jie Song ◽  
Cheng-Yong Wang ◽  
Yuan Yang ◽  
Jin-Heng Li

The metal-free and facile synthesis of ynones via carbonyl C(sp2)–H oxidative alkynylation of aldehydes with enynyl benziodoxolones is presented.


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