Functionalization of α-hydroxyphosphonates as a convenient route toN-tosyl-α-aminophosphonates-Reference-Cited by-同舟云学术

Functionalization of α-hydroxyphosphonates as a convenient route toN-tosyl-α-aminophosphonates

Published:2018 Issue:22 Volume:8 Page:11957-11974
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Cytlak Tomasz¹²³⁴⁵^ORCID,Skibińska Monika¹²³⁴^ORCID,Kaczmarek Patrycja¹²³⁴,Kaźmierczak Marcin¹²³⁴⁵^ORCID,Rapp Magdalena¹²³⁴,Kubicki Maciej¹²³⁴,Koroniak Henryk¹²³⁴

Affiliation:

1. Faculty of Chemistry

2. Adam Mickiewicz University in Poznań

3. 61-614 Poznań

4. Poland

5. Centre for Advanced Technologies

Abstract

The reaction mechanism and diastereoselectivity of the direct transformation of α-hydroxyphosphonates6a,b–21a,bbypara-toluenesulfonamide, yielding α-(N-tosyl)aminophosphonates23a,b–37a,bunder K₂CO₃conditions are presented.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/RA/C8RA01656A

Reference109 articles.

1. Inactivation of the Enterobacter cloacae P99 .beta.-Lactamase by a Fluorescent Phosphonate: Direct Detection of Ligand Binding at the Second Site

2. Structural Insight into the Stereoselective Inhibition of MMP-8 by Enantiomeric Sulfonamide Phosphonates

3. Phosphonate analogues of acidic amino acids: inhibition of excitatory amino acid transmitter binding to cerebellar membranes and of the stimulation of cerebellar cyclic GMP levels

4. N-(Phosphonoacetyl)amino phosphonates. Phosphonate analogs of N-(phosphonoacetyl)-L-aspartic acid (PALA)

5. Inhibition of aminopeptidases by aminophosphonates

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