Recent advances in theoretical calculations of indirect spin–spin coupling constants
LB Krivdin, RH Contreras - Annual Reports on NMR Spectroscopy, 2007 - Elsevier
Recent trends in theoretical calculations of indirect spin–spin coupling constants covering
the period of May 2003–July 2006 are outlined with the emphasis on the currently used …
the period of May 2003–July 2006 are outlined with the emphasis on the currently used …
Zwitterionic glycosidase inhibitors: salacinol and related analogues
S Mohan, BM Pinto - Carbohydrate Research, 2007 - Elsevier
Natural products with interesting biological properties and structural diversity have often
served as valuable lead drug candidates for the treatment of human diseases. Salacinol, a …
served as valuable lead drug candidates for the treatment of human diseases. Salacinol, a …
Stereoselective C-Glycosylation Reactions of Pyranoses: The Conformational Preference and Reactions of the Mannosyl Cation
CG Lucero, KA Woerpel - The Journal of Organic Chemistry, 2006 - ACS Publications
A systematic study of C-glycosylations of acetals related to mannose and other pyranoses
was conducted. The C-5 alkoxyalkyl group provides only a modest influence on …
was conducted. The C-5 alkoxyalkyl group provides only a modest influence on …
Electrostatic interactions in cations and their importance in biology and chemistry
DM Smith, KA Woerpel - Organic & Biomolecular Chemistry, 2006 - pubs.rsc.org
Electrostatic effects exert strongly stabilizing influences on cations, in many cases controlling
the conformational preferences of these cations. The lowest energy conformers are ones …
the conformational preferences of these cations. The lowest energy conformers are ones …
Biological evaluation of de-O-sulfonated analogs of salacinol, the role of sulfate anion in the side chain on the α-glucosidase inhibitory activity
G Tanabe, K Yoshikai, T Hatanaka… - Bioorganic & medicinal …, 2007 - Elsevier
De-O-sulfonated analogs (10a, Y−= CH3OSO3 and 10b, Y−= Cl) of salacinol, a naturally
occurring glycosidase inhibitor, and its diastereomer (12a, Y−= CH3OSO3) with l-thiosugar …
occurring glycosidase inhibitor, and its diastereomer (12a, Y−= CH3OSO3) with l-thiosugar …
Reconciling solvent effects on rotamer populations in carbohydrates A joint MD and NMR analysis
J Gonzalez-Outeiriño, KN Kirschner… - Canadian journal of …, 2006 - cdnsciencepub.com
Il est bien connu que les préférences rotationnelles des groupes hydroxyméthyles des
pyranosides dépend de l'environnement local que ce soit à l'état solide, en solution ou en …
pyranosides dépend de l'environnement local que ce soit à l'état solide, en solution ou en …
Rational Design and Expedient Synthesis of Heparan Sulfate Mimetics from Natural Aminoglycosides for Structure and Activity Relationship Studies
Heparan sulfate (HS) contains variably repeating disaccharide units organized into high‐
and low‐sulfated domains. This rich structural diversity enables HS to interact with many …
and low‐sulfated domains. This rich structural diversity enables HS to interact with many …
Indolizidine and quinolizidine alkaloids
JP Michael - Natural product reports, 2005 - pubs.rsc.org
Covering: July 2003 to June 2004. Previous review: Nat. Prod. Rep., 2004, 21, 625. This
review covers the isolation, structure determination, synthesis, chemical transformations and …
review covers the isolation, structure determination, synthesis, chemical transformations and …
New chain-extended analogues of salacinol and blintol and their glycosidase inhibitory activities. Mapping the active-site requirements of human maltase …
The synthesis of new chain-extended sulfonium and selenonium salts of 1, 4-anhydro-4-thio-
(or 4-seleno)-d-arabinitol, analogues of the naturally occurring glycosidase inhibitor …
(or 4-seleno)-d-arabinitol, analogues of the naturally occurring glycosidase inhibitor …
Combined Chemical, Biological and Theoretical DFT‐QTAIM Study of Potent Glycosidase Inhibitors Based on Quaternary Indolizinium Salts
P Šafář, J Žúžiová, Š Marchalín… - European Journal of …, 2012 - Wiley Online Library
Six novel enantiopure epimeric indolizidinediols have been easily prepared in high yields
by an effective and well‐established regioselective THF ring‐opening reaction as a key step …
by an effective and well‐established regioselective THF ring‐opening reaction as a key step …