Selective functionalization of silyl thiazolidines leads to different heterocyclic systems. Their is strictly dependent on the nature of the protecting group present on the nitrogen and the substituents on the heterocyclic ring, as well as the reaction conditions and the nature of the aldehyde, leading selectively to the formation of -hydroxy thiazolidines or fused oxazolidinones.

Selective access to mono- and polycyclic sulfur containing heterocycles through silyl thiazolidines functionalization / Antonella Capperucci; Alessandro Degl’Innocenti; Caterina Tiberi; Salvatore Pollicino; Irene Malesci. - STAMPA. - OR29:(2008), pp. 33-33. (Intervento presentato al convegno 23nd International Symposium on the Organic Chemistry of Sulfur (ISOCS-23) tenutosi a Mosca (Russia) nel 29 Giugno-4 Luglio 2008).

Selective access to mono- and polycyclic sulfur containing heterocycles through silyl thiazolidines functionalization

CAPPERUCCI, ANTONELLA;
2008

Abstract

Selective functionalization of silyl thiazolidines leads to different heterocyclic systems. Their is strictly dependent on the nature of the protecting group present on the nitrogen and the substituents on the heterocyclic ring, as well as the reaction conditions and the nature of the aldehyde, leading selectively to the formation of -hydroxy thiazolidines or fused oxazolidinones.
2008
23nd International Symposium on the Organic Chemistry of Sulfur (ISOCS-23)
23nd International Symposium on the Organic Chemistry of Sulfur (ISOCS-23)
Mosca (Russia)
Antonella Capperucci; Alessandro Degl’Innocenti; Caterina Tiberi; Salvatore Pollicino; Irene Malesci
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/876967
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