Advances in the synthesis of (3<i>R</i>,3a<i>S</i>,6a<i>R</i>)-hexahydrofuro[2,3-<i>b</i>]furan-3-ol, a key ligand of the HIV protease inhibitors

Авторы

  • Mengqi Dong College of Chemical Engineering, Qingdao University of Science and Technology
  • Dawei Teng College of Chemical Engineering, Qingdao University of Science and Technology
  • Guorui Cao College of Chemical Engineering, Qingdao University of Science and Technology

Ключевые слова:

bis-THF alcohol, HIV protease inhibitors, asymmetric metal catalysis, chiral-substrate-induced reaction, enzyme-catalyzed resolution

Аннотация

(3R,3aS,6aR)-Hexahydrofuro[2,3-b]furan-3-ol (bis-THF alcohol) is a key intermediate for the synthesis of HIV protease inhibitors with lower toxicity and better drug resistance. Due to its unique structure with three chiral centers and the high cost of this double-ring compound, chemists have paid much attention to the development of new synthetic routes. Based on the sources of the chiral carbon in bis-THF alcohol, this work systematically summarizes the existing synthetic processes using enzyme-catalyzed resolution, asymmetric metal catalysis, and chiral-substrate-induced reactions.

 

Биографии авторов

Mengqi Dong, College of Chemical Engineering, Qingdao University of Science and Technology

College of Chemical Engineering, Qingdao University of Science and Technology,
Qingdao 266042, China

Dawei Teng, College of Chemical Engineering, Qingdao University of Science and Technology

College of Chemical Engineering, Qingdao University of Science and Technology,
Qingdao 266042, China

Guorui Cao, College of Chemical Engineering, Qingdao University of Science and Technology

College of Chemical Engineering, Qingdao University of Science and Technology,
Qingdao 266042, China

Опубликован

2024-09-25

Выпуск

Раздел

Обзорные статьи