scholarly journals Catalytic enantioselective intramolecular Tishchenko reaction of meso-dialdehyde: synthesis of (S)-cedarmycins

RSC Advances ◽  
2021 ◽  
Vol 11 (19) ◽  
pp. 11606-11609
Author(s):  
Ismiyarto ◽  
Nobuki Kishi ◽  
Yuki Adachi ◽  
Rui Jiang ◽  
Takahiro Doi ◽  
...  

The first successful example of a catalytic enantioselective intramolecular Tishchenko reaction of a meso-dialdehyde in the presence of a chiral iridium complex is described.

2008 ◽  
Vol 8 (3-4) ◽  
pp. 490-493 ◽  
Author(s):  
Hui Wang ◽  
Jeong-Tak Ryu ◽  
Minhyeon Song ◽  
Younghwan Kwon

Author(s):  
Genki Toyooka ◽  
Toshiki Tanaka ◽  
Kenji Kitayama ◽  
Naoko Kobayashi ◽  
Takashi Watanabe ◽  
...  

A new and simple method for hydrogen production from cellulose using an iridium catalyst and an ionic liquid under mild conditions was developed.


2021 ◽  
Vol 86 (5) ◽  
pp. 4296-4303
Author(s):  
Aneta Turlik ◽  
Kaori Ando ◽  
Pamela Mackey ◽  
Emma Alcock ◽  
Mark Light ◽  
...  
Keyword(s):  

2021 ◽  
Author(s):  
Liang Hao ◽  
Yan-Mei Zhong ◽  
Cai-Ping Tan ◽  
Zong-Wan Mao

A phosphorescent Ir(iii) complex was developed as viscosity probe for realtime tracking of endoplasmic reticulum during ferroptosis.


Author(s):  
Ruixia Liu ◽  
Jingkuo Han ◽  
Bin Li ◽  
Xian Liu ◽  
Zhao Wei ◽  
...  

A highly efficient intramolecular asymmetric reductive amination transformation catalyzed by an iridium complex of tBu-ax-Josiphos has been realized, providing an efficient access to various THIQ alkaloids.


Catalysts ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 891
Author(s):  
Ken-ichi Fujita ◽  
Takayoshi Inoue ◽  
Toshiki Tanaka ◽  
Jaeyoung Jeong ◽  
Shohichi Furukawa ◽  
...  

A new catalytic system has been developed for hydrogen production from various monosaccharides, mainly glucose, as a starting material under reflux conditions in water in the presence of a water-soluble dicationic iridium complex bearing a functional bipyridine ligand. For example, the reaction of D-glucose in water under reflux for 20 h in the presence of [Cp*Ir(6,6′-dihydroxy-2,2′-bipyridine)(H2O)][OTf]2 (1.0 mol %) (Cp*: pentamethylcyclopentadienyl, OTf: trifluoromethanesulfonate) resulted in the production of hydrogen gas in 95% yield. In the present catalytic reaction, it was experimentally suggested that dehydrogenation of the alcoholic moiety at 1-position of glucose proceeded.


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