Aromatic Dienophiles. 1. A Theoretical Study of an Inverse-Electron Demand Diels−Alder Reaction between 2-Aminopyrrole and 1,3,5-Triazine

2001 ◽  
Vol 66 (18) ◽  
pp. 6029-6036 ◽  
Author(s):  
Zhi-Xiang Yu ◽  
Qun Dang ◽  
Yun-Dong Wu
RSC Advances ◽  
2015 ◽  
Vol 5 (113) ◽  
pp. 93318-93330 ◽  
Author(s):  
Weiyi Li ◽  
Na Yang ◽  
Yajing Lv

The enantioselectivity originates from the hindrance of a BINOL ligand, and the exo-selectivity is achieved by the favored electrophilic/nucleophilic interaction.


2017 ◽  
Vol 41 (21) ◽  
pp. 12392-12396 ◽  
Author(s):  
Siting Ni ◽  
Jun Zhu ◽  
Mohamed Amine Mezour ◽  
R. Bruce Lennox

A thermally-mild method for covalent binding of SWCNTs to AuNRs, based on an inverse-electron-demand Diels–Alder reaction, is established and discussed.


2021 ◽  
Author(s):  
Tingting Zhou ◽  
Anquan Zheng ◽  
Luqiong Huo ◽  
Changgeng Li ◽  
Haibo Tan ◽  
...  

Driven by bioinspiration and appreciation of the structure of ericifolione, a biomimetic tautomerization/intermolecular inverse-electron-demand hetero Diels-Alder reaction cascade sequence promoted by sodium acetate to rapidly construct sterically hindered dihydropyran scaffolds...


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