ChemInform Abstract: Enantioselective Synthesis of Dihydrocoumarin Derivatives by Chiral Scandium(III)-Complex Catalyzed Inverse-Electron-Demand hetero-Diels-Alder Reaction.

ChemInform ◽  
2015 ◽  
Vol 46 (28) ◽  
pp. no-no
Author(s):  
Haipeng Hu ◽  
Yangbin Liu ◽  
Jing Guo ◽  
Lili Lin ◽  
Yali Xu ◽  
...  
Keyword(s):  
Alder Reaction ◽  
Diels Alder ◽  
Enantioselective Synthesis ◽  
Inverse Electron Demand ◽  
Diels Alder Reaction ◽  
Electron Demand

Enantioselective Synthesis of cis ‐Decalin Derivatives by the Inverse‐Electron‐Demand Diels–Alder Reaction of 2‐Pyrones

2020 ◽  
Vol 132 (42) ◽  
pp. 18570-18575
Author(s):  
Xu‐Ge Si ◽  
Zhi‐Mao Zhang ◽  
Cheng‐Gong Zheng ◽  
Zhan‐Ting Li ◽  
Quan Cai
Keyword(s):  
Alder Reaction ◽  
Diels Alder ◽  
Enantioselective Synthesis ◽  
Inverse Electron Demand ◽  
Diels Alder Reaction ◽  
Electron Demand

Enantioselective synthesis of dihydrocoumarin derivatives by chiral scandium(iii)-complex catalyzed inverse-electron-demand hetero-Diels–Alder reaction

2015 ◽  
Vol 51 (18) ◽  
pp. 3835-3837 ◽  
Author(s):  
Haipeng Hu ◽  
Yangbin Liu ◽  
Jing Guo ◽  
Lili Lin ◽  
Yali Xu ◽  
...  
Keyword(s):  
Alder Reaction ◽  
Diels Alder ◽  
Enantioselective Synthesis ◽  
Quinone Methides ◽  
Inverse Electron Demand ◽  
Diels Alder Reaction ◽  
Electron Demand

An asymmetric inverse-electron-demand hetero-Diels–Alder reaction between o-quinone methides and azlactones to generate potentially pharmacological active dihydrocoumarins has been achieved efficiently by using a chiral N,N′-dioxide–Sc(iii) complex as the catalyst.

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