Synthesis of Cyclohexane-Fused Isocoumarins via Cationic Palladium(II)-Catalyzed Cascade Cyclization Reaction of Alkyne-Tethered Carbonyl Compounds Initiated by Intramolecular Oxypalladation of Ester-Substituted Aryl Alkynes

2016 ◽  
Vol 81 (8) ◽  
pp. 3423-3429 ◽  
Author(s):  
Jianbo Zhang ◽  
Xiuling Han ◽  
Xiyan Lu
ChemInform ◽  
2013 ◽  
Vol 44 (37) ◽  
pp. no-no
Author(s):  
Elena Yu. Schmidt ◽  
Ivan A. Bidusenko ◽  
Nadezhda I. Protsuk ◽  
Igor A. Ushakov ◽  
Boris A. Trofimov

2021 ◽  
Vol 19 (37) ◽  
pp. 8086-8095
Author(s):  
Wenzhong Li ◽  
Yu Wang ◽  
Huijing Qi ◽  
Ran Shi ◽  
Jiazhu Li ◽  
...  

Metal-free cascade cyclization of 2-acylbenzoic acids with amines provided a one-pot synthesis of diverse isoindoloisoquinoline and benzoindolizinoindole derivatives, which were subsequently used to produce nitrogen-containing nine-membered ring compounds.


2019 ◽  
Vol 60 (2) ◽  
pp. 187-190 ◽  
Author(s):  
Kentaro Wada ◽  
Noriyuki Kogure ◽  
Mariko Kitajima ◽  
Hiromitsu Takayama

2008 ◽  
Vol 49 (22) ◽  
pp. 3592-3595 ◽  
Author(s):  
Xianhai Huang ◽  
Ning Shao ◽  
Anandan Palani ◽  
Robert Aslanian ◽  
Alexei Buevich ◽  
...  

Synlett ◽  
2019 ◽  
Vol 30 (15) ◽  
pp. 1810-1814 ◽  
Author(s):  
Enoch A. Mensah ◽  
Shawn D. Green ◽  
Jesse West ◽  
Tyler Kindoll ◽  
Brenda Lazaro-Martinez

The development of a new, highly efficient, and simple method for masking carbonyl groups as acetals and ketals is described. This methodology relies on the nature of the palladium catalyst to direct the acetalization/ketalization reaction. This new protocol is mild and proceed with a very low catalyst loading at ambient temperatures. The method has been extended to a wide variety of different carbonyl compounds with various steric encumbrances to form the corresponding acetals and ketals in excellent yields.


2020 ◽  
Vol 132 (45) ◽  
pp. 20295-20303
Author(s):  
Tomas Javorskis ◽  
Ieva Karpavičienė ◽  
Arminas Jurys ◽  
Gustautas Snarskis ◽  
Rita Bukšnaitienė ◽  
...  

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