Chiral Transition Metal Lewis Acids Bearing Bis(oxazolinyl)phenyl (Phebox) as a Pincer Ligand: Synthesis and Application for the Asymmetric Reactions

ChemInform ◽  
2003 ◽  
Vol 34 (35) ◽  
Author(s):  
Yukihiro Motoyama ◽  
Hisao Nishiyama
2018 ◽  
Vol 47 (44) ◽  
pp. 15725-15736 ◽  
Author(s):  
Konstantina Pringouri ◽  
Muhammad U. Anwar ◽  
Liz Mansour ◽  
Nathan Doupnik ◽  
Yassine Beldjoudi ◽  
...  

The synthesis and coordination chemistry of ligand LH2 to first row transition metals is described in which it acts as a tridentate N,N′,N′′-donor.


Synthesis ◽  
2021 ◽  
Author(s):  
Heather Lam ◽  
Mark Lautens ◽  
Xavier Abel-Snape ◽  
Martin F. Köllen

Abstract(4+3)-Annulations are incredibly versatile reactions which combine a 4-atom synthon and a 3-atom synthon to form both 7-membered carbocycles as well as heterocycles. We have previously reviewed transition-metal-catalyzed (4+3)-annulations. In this review, we will cover examples involving bases, NHCs, phosphines, Lewis and Brønsted acids as well as some rare examples of boronic acid catalysis and photocatalysis. In analogy to our previous review, we exclude annulations involving cyclic dienes like furan, pyrrole, cyclohexadiene or cyclopentadiene, as Chiu, Harmata, Fernándes and others have recently published reviews encompassing such substrates. We will however discuss the recent additions (2010–2020) to the literature on (4+3)-annulations involving other types of 4-atom-synthons.1 Introduction2 Bases3 Annulations Using N-Heterocyclic Carbenes3.1 N-Heterocyclic Carbenes (NHCs)3.2 N-Heterocyclic Carbenes and Base Dual-Activation4 Phosphines5 Acids5.1 Lewis Acids5.2 Brønsted Acids6 Boronic Acid Catalysis and Photocatalysis7 Conclusion


2011 ◽  
Vol 7 ◽  
pp. 570-577 ◽  
Author(s):  
Sami F Tlais ◽  
Gregory B Dudley

A highly efficient synthesis of oxygenated 5,5-spiroketals was performed towards the synthesis of the cephalosporolides. Gold(I) chloride in methanol induced the cycloisomerization of a protected alkyne triol with concomitant deprotection to give a strategically hydroxylated 5,5-spiroketal, despite the potential for regiochemical complications and elimination to furan. Other late transition metal Lewis acids were less effective. The use of methanol as solvent helped suppress the formation of the undesired furan by-product. This study provides yet another example of the advantages of gold catalysis in the activation of alkyne π-systems.


2021 ◽  
Author(s):  
Yihan Cao ◽  
Wei-Chun Shih ◽  
Nattamai Bhuvanesh ◽  
Jia Zhou ◽  
Oleg V Ozerov

Pyridine and quinoline undergo selective C-H activation in the 2-position with Rh and Ir complexes of a boryl/bis(phosphine) PBP pincer ligand, resulting in a 2-pyridyl bridging the transition metal and...


2017 ◽  
Vol 53 (75) ◽  
pp. 10366-10369 ◽  
Author(s):  
Shaoyu Mai ◽  
Changqing Rao ◽  
Ming Chen ◽  
Jihu Su ◽  
Jiangfeng Du ◽  
...  

Novel catalytic systems consisting of cationic gold complexes, N-hydroxyphthalimide (NHPI), and transition-metal-based Lewis acids have been developed for the one-pot synthesis of functionalized oxazoles.


2016 ◽  
Vol 16 (5) ◽  
pp. 2405-2425 ◽  
Author(s):  
Wei Guan ◽  
Guixiang Zeng ◽  
Hajime Kameo ◽  
Yoshiaki Nakao ◽  
Shigeyoshi Sakaki

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