Enantioselective synthesis of substituted α-aminophosphonates catalysed by d-glucose-based crown ethers: pursuit of the origin of stereoselectivity-Reference-Cited by-同舟云学术

Enantioselective synthesis of substituted α-aminophosphonates catalysed by d-glucose-based crown ethers: pursuit of the origin of stereoselectivity

Published:2017 Issue:24 Volume:41 Page:14945-14953
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Pham Son Truong¹²³⁴⁵,Rapi Zsolt¹²³⁴⁵,Bakó Péter¹²³⁴⁵,Petneházy Imre¹²³⁴⁵,Stirling András⁶⁷⁸⁹⁵^ORCID,Jászay Zsuzsa¹²³⁴⁵

Affiliation:

1. Department of Organic Chemistry and Technology

2. Budapest University of Technology and Economics

3. PO Box 91

4. Budapest 1521

5. Hungary

6. Institute of Organic Chemistry

7. Research Centre for Natural Sciences

8. Hungarian Academy of Sciences

9. Budapest

Abstract

Tuning the electronic properties of the catalyst can control the enantioselectivity of d-glucose-based crown ethers by a simple mechanism.

Funder

Országos Tudományos Kutatási Alapprogramok

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2017/NJ/C7NJ03345A

Reference64 articles.

1. J. Oleksyszyn , in Aminophosphonic and Aminophosphinic Acids , ed. V. P. Kukhar and H. R. Hudson , John Wiley and Sons , Chichester , 2000 , ch. 15, pp. 537–558

2. BIOLOGICAL ACTIVITY OF AMINOPHOSPHONIC ACIDS

3. Aminophosphonic Acids - Phosphorus Analogues of Natural Amino Acids.Part 1: Syntheses of α-Aminophosphonic Acids

4. Design of Biomimetic Catalysts by Molecular Imprinting in Synthetic Polymers: The Role of Transition State Stabilization

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