RNA–peptide conjugate synthesis by inverse-electron demand Diels–Alder reaction

2014 ◽  
Vol 12 (26) ◽  
pp. 4701-4707 ◽  
Author(s):  
Sandeep Ameta ◽  
Juliane Becker ◽  
Andres Jäschke

We present an efficient method to synthesize RNA–peptide conjugates employing inverse Diels–Alder cycloaddition. Different dienophiles are enzymatically incorporated into RNA and then conjugated with a tetrazine peptide at 1 : 1 stoichiometry.

2016 ◽  
Vol 24 (11) ◽  
pp. 2589-2594 ◽  
Author(s):  
Mi Hee Choi ◽  
Ha Eun Shim ◽  
Seong-Jae Yun ◽  
Hye Rim Kim ◽  
Sajid Mushtaq ◽  
...  

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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