A strategy featuring a key retrosynthetic disconnection at the C2-C3 position was applied to the total synthesis of the common diterpenoid tricyclic skeleton of sarcodictyins and eleutherobin. Fully functionalized cyclization precursors were accessed via a brief and convergent route, making use of unprecedented synthetic transformations. (C) 2001 Elsevier Science Ltd. All rights reserved.

Synthetic studies on the sarcodictyins: synthesis of fully functionalized cyclization precursors / S.M. Ceccarelli, U. Piarulli, C.M.A. Gennari. - In: TETRAHEDRON. - ISSN 0040-4020. - 57:40(2001), pp. 8531-8542.

Synthetic studies on the sarcodictyins: synthesis of fully functionalized cyclization precursors

C.M.A. Gennari
Ultimo
2001

Abstract

A strategy featuring a key retrosynthetic disconnection at the C2-C3 position was applied to the total synthesis of the common diterpenoid tricyclic skeleton of sarcodictyins and eleutherobin. Fully functionalized cyclization precursors were accessed via a brief and convergent route, making use of unprecedented synthetic transformations. (C) 2001 Elsevier Science Ltd. All rights reserved.
Settore CHIM/06 - Chimica Organica
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/175585
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