Many of the symbols used in stereochemical nomenclature are mentioned but details of their
assignment or their incorporation into chemical names are left to the appropriate …

Two benzylidene derivatives anisaldehyde-cyanoguanidine imine (CMBG) and p–
dimethylaminobenzaldehyde-TRIS imine (DBHP) were prepared according to the 12 …

Some important results from the past seven years on the ring‐chain tautomerism of 1, 3‐
heterocycles are reviewed, including substituent effects on the tautomeric equilibria and …

In vivo phosphorylation of FTY720 (1) in rats and humans resulted exclusively in the
biologically active (S)-configured enantiomer, which was proven by an ex vivo o …

High-yield regioselective synthesis of imines and oxazolidines derivatives of 2-amino-1, 3-
propandiol (serinol) was achieved by performing the reaction with aldehydes and ketones …

The reverse anomeric effect is usually associated with the equatorial preference of nitrogen
substituents at the anomeric center. Once postulated as another anomeric effect with …

The review covers the use of chemical shifts, isotope effects on chemical shifts and coupling
constants in the description of Schiff bases. o-Hydroxy Schiff bases are often tautomeric and …

Hydrogen atom abstraction from the C5 '-position of nucleotides in DNA results in direct
strand scission. The newly formed 5 '-termini of the cleaved DNA consists of alkali-labile …

A curious and noticeable structural feature in Schiff bases from 2-aminoaldoses is the fact
that imino tautomers arranged equatorially in the most stable ring conformation exhibit a …

This paper thoroughly explores the formation of Schiff bases derived from salicylaldehydes
and a conformationally restricted amino alcohol (1-amino-2-indanol), as well as the …