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Updated: Sep 28, 2026

A Customizable Approach for the Enzymatic Production and Purification of Diterpenoid Natural Products
Published on: October 4, 2019
Structure and absolute configuration of new diterpenes from Lavandula multifida
Matteo Politi1, Nunziatina De Tommasi, Gennaro Pescitelli
1Dipartimento di Chimica Bioorganica e Biofarmacia, Università di Pisa, Via Bonanno 33, 56126 Pisa, Italy.
Abstract:
Four new diterpenes (1-4) have been isolated from the aerial parts of Lavandula multifida, together with the known compound glutinosin (5). The structures of these compounds were identified on the basis of extensive NMR studies as 15,16-dihydroxy-7,11-dioxopimar-8(9)-ene (1), 15S,16-dihyroxy-7-oxopimar-8(9)-ene (2), 15,16,17-trihydroxy-7-oxopimar-8(9)-ene (3), and 15,16,17-trihydroxypimar-8(9)-ene (4). The absolute configuration of the 15,16-diol moiety in 1-5 was determined observing the circular dichroism induced after addition of dimolybdenum tetracetate in DMSO solution.
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