A one-pot synthetic method for the hetero-bifunctionalization of α-cyclodextrin at the secondary hydroxyl side with high clockwise–counterclockwise selectivity

Author:

Huang Xi12345,Yasunaga Shun1234,Fukudome Makoto1234,Chen Wen-Hua56789ORCID,Yuan De-Qi1234ORCID

Affiliation:

1. Faculty of Pharmaceutical Sciences

2. Kobe Gakuin University

3. Kobe 650-8586

4. Japan

5. Guangdong Provincial Key Laboratory of New Drug Screening

6. School of Pharmaceutical Sciences

7. Southern Medical University

8. Guangzhou 510515

9. P. R. China

Abstract

The first one-pot synthetic method has been established to ensure the sequence-selective, highly efficient introduction of two different functionalities into the secondary side of α-cyclodextrin.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference30 articles.

1. Recent progress in the design and synthesis of artificial enzymes

2. Biomimetic Reactions Catalyzed by Cyclodextrins and Their Derivatives

3. C. M. Pedersen and M.Bols, Cyclodextrin-based artificial enzymes: synthesis and function, in Organic Synthesis and Molecular Engineering, ed. M. B. Nielsen, Wiley, 2013, ch. 11, pp. 305–332

4. Metal complexes of functionalized cyclodextrins as enzyme models and chiral receptors

5. Complexation Thermodynamics of Cyclodextrins

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