Настоящая книга предназначена для студентов, аспирантов-химиков и научных
сотрудников, специализирующихся в области тонкого органического синтеза, и …

Facile methods are described for accessing four diastereomerically pure 3-mercaptoaspartic
acid derivative from l-aspartic acid. In our synthesis, ring-opening reactions of oxazoline-4, 5 …

A novel and efficient microwave-assisted one-step reaction was developed to synthesize
chiral N-sulfonylaziridines by the reaction of different chiral amino alcohols and sulfonic …

Résumé Le gel de silice, l'alumine neutre et les argiles activées à l'acide transforment les N-
acyl-2, 2-diméthylaziridines 1 en un mélange de N-méthallylamides 2, d'oxazolines 3 et …

We successfully isolated a spiro imidazolidine-oxazolidine intermediate in the reaction of
guanidinium ylide mediated aziridination using α-bromocinnamaldehyde. X-ray …

A tandem approach for the regio-and stereoselective synthesis of oxazolo-fused
pyrroloquinolines 3a–l via the reaction of o-alkynylaldehydes 1a–i with chiral amino …

The treatment of a range of N-and O-enones derived from various camphor-based chiral
auxiliaries A–D with N-aminophthalimide in the presence of lead tetraacetate is described …

An approach to 3-bromo-4-alkyl-6-aryl-5, 6-dihydropyridin-2-ones and 3-bromo-5-ethyl-6-
aryl-5, 6-dihydropyridin-2-ones starting from β, γ-unsaturated α-bromoketenes and imines is …

TFA). The investigations were based on a set of 22 (Z)-and (E)-N-acyl-a, b-dehydro-a-amino
acid esters of diverse structures, with aliphatic, aromatic and heteroaromatic substituents at …

Publisher Summary This chapter is a sequel to eight reviews already published in Advances
in Heterocyclic Chemistry. It includes monographs and reviews published during the period …