The stereoselective synthesis of an advanced intermediate of Taxuspine U and X has been accomplished using a ring closing metathesis strategy. The feasibility of ring closing metathesis in synthesizing highly constrained and functionalized macrocycles has been demonstrated provided the appropriate substrate structure and substitution pattern are chosen. © 2006 Elsevier Ltd. All rights reserved.
Galletti, E., Avramova, S.I., Renzulli, M.L., Corelli, F., Botta, M. (2007). Stereoselective synthesis of advanced intermediates en route to Taxuspine U and X: a study of macrocyclization via ring closing metathesis to highly constrained twelve-membered rings. TETRAHEDRON LETTERS, 48(5), 751-754 [10.1016/j.tetlet.2006.11.167].
Stereoselective synthesis of advanced intermediates en route to Taxuspine U and X: a study of macrocyclization via ring closing metathesis to highly constrained twelve-membered rings
Galletti, Elena;Renzulli, M. L.;Corelli, Federico;Botta, Maurizio
2007-01-01
Abstract
The stereoselective synthesis of an advanced intermediate of Taxuspine U and X has been accomplished using a ring closing metathesis strategy. The feasibility of ring closing metathesis in synthesizing highly constrained and functionalized macrocycles has been demonstrated provided the appropriate substrate structure and substitution pattern are chosen. © 2006 Elsevier Ltd. All rights reserved.
| File | Dimensione | Formato | |
|---|---|---|---|
|
1-s2.0-S004040390602404X-main.pdf
non disponibili
Tipologia:
Post-print
Licenza:
NON PUBBLICO - Accesso privato/ristretto
Dimensione
142.01 kB
Formato
Adobe PDF
|
142.01 kB | Adobe PDF | Visualizza/Apri Richiedi una copia |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
https://hdl.handle.net/11365/3812
Attenzione
Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo