One-Pot Protocol to Functionalized Benzopyrrolizidine Catalyzed Successively by Rh2(OAc)4 and Cu(OTf)2: A Transition Metal–Lewis Acid Catalysis Relay

2014 ◽  
Vol 17 (1) ◽  
pp. 66-69 ◽  
Author(s):  
Hua-Dong Xu ◽  
Zhi-Hong Jia ◽  
Ke Xu ◽  
Hao Zhou ◽  
Mei-Hua Shen
Keyword(s):  
Transition Metal ◽  
Lewis Acid ◽  
Acid Catalysis ◽  
Lewis Acid Catalysis ◽  
One Pot

Merging gold catalysis, organocatalytic oxidation, and Lewis acid catalysis for chemodivergent synthesis of functionalized oxazoles from N-propargylamides

2017 ◽  
Vol 53 (75) ◽  
pp. 10366-10369 ◽  
Author(s):  
Shaoyu Mai ◽  
Changqing Rao ◽  
Ming Chen ◽  
Jihu Su ◽  
Jiangfeng Du ◽  
...  
Keyword(s):  
Transition Metal ◽  
Lewis Acid ◽  
Lewis Acids ◽  
Acid Catalysis ◽  
Gold Catalysis ◽  
One Pot ◽  
Catalytic Systems ◽  
One Pot Synthesis ◽  
The One ◽  
Cationic Gold

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.

scholarly journals Enantioselective one-pot synthesis of dihydroquinolones via BINOL-derived Lewis acid catalysis

2014 ◽  
Vol 12 (28) ◽  
pp. 5094-5097 ◽  
Author(s):  
Peter C. Knipe ◽  
Martin D. Smith
Keyword(s):  
Lewis Acid ◽  
Acid Catalysis ◽  
Lewis Acid Catalysis ◽  
One Pot ◽  
One Pot Synthesis

A high-yielding and diastereoselective route to biologically significant 2-aryl- and 2-alkyl-3-amido dihydroquinolones has been developed in up to 90 : 10 e.r. by employing a novel Lewis acidic BINOL-derived copper(ii) catalyst.

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