Conformational and configurational study of 2-phenyl-4-aryl-1,3,2-dioxaphosphonates derived from xylofuranose derivatives. The anomeric effect in the spontaneous isomerization of cyclic phosphonates-Reference-Cited by-同舟云学术

Conformational and configurational study of 2-phenyl-4-aryl-1,3,2-dioxaphosphonates derived from xylofuranose derivatives. The anomeric effect in the spontaneous isomerization of cyclic phosphonates

Published:2012-08 Issue:35 Volume:53 Page:4727-4732
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Quintero Leticia,Höpfl Herbert,Sosa-Rivadeneyra Martha,Ortiz Aurelio,Meza-León Rosa L.,Cruz-Gregorio Silvano,Sartillo-Piscil Fernando

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

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5. Design, Synthesis, and Characterization of a Series of Cytochrome P450 3A-Activated Prodrugs (HepDirect Prodrugs) Useful for Targeting Phosph(on)ate-Based Drugs to the Liver§

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1. Further Evidence on the Favorable Role of the Anomeric Effect on the Cleavage of HepDirect and Cyclophosphamide Prodrugs;The Journal of Organic Chemistry;2014-10-03

2. Generalized anomeric effect of α-chloro-O-oxime ethers; influence of various substitutions by DFT, NBO and AIM studies;Computational and Theoretical Chemistry;2014-02

3. Chapter 9. Physical methods;Organophosphorus Chemistry;2014