Isolation and chemistry of clerodane diterpenes from Dodonaea ceratocarpa

V.N. Moussa; Brian Skelton; A.D. Payne

doi:10.1016/j.tet.2016.09.062

Isolation and chemistry of clerodane diterpenes from Dodonaea ceratocarpa

V.N. Moussa, Brian Skelton, A.D. Payne

Centre for Microscopy, Characterisation & Analysis

Research output: Contribution to journal › Article › peer-review

4 Citations (Scopus)

Abstract

© 2016 Elsevier LtdA new clerodane was isolated from Dodonaea ceratocarpa and obtained in appreciable quantities (0.5% w/w plant). A variety of reactions on this clerodane provided access to a range of new derivatives, including cationic skeletal rearrangements and reduction reactions with lanthanide salt additives.

Original language	English
Pages (from-to)	7470-7480
Number of pages	11
Journal	Tetrahedron
Volume	72
Issue number	47
DOIs	https://doi.org/10.1016/j.tet.2016.09.062
Publication status	Published - 2016

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title = "Isolation and chemistry of clerodane diterpenes from Dodonaea ceratocarpa",

abstract = "{\textcopyright} 2016 Elsevier LtdA new clerodane was isolated from Dodonaea ceratocarpa and obtained in appreciable quantities (0.5% w/w plant). A variety of reactions on this clerodane provided access to a range of new derivatives, including cationic skeletal rearrangements and reduction reactions with lanthanide salt additives.",

author = "V.N. Moussa and Brian Skelton and A.D. Payne",

year = "2016",

doi = "10.1016/j.tet.2016.09.062",

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AU - Moussa, V.N.

AU - Skelton, Brian

AU - Payne, A.D.

PY - 2016

Y1 - 2016

N2 - © 2016 Elsevier LtdA new clerodane was isolated from Dodonaea ceratocarpa and obtained in appreciable quantities (0.5% w/w plant). A variety of reactions on this clerodane provided access to a range of new derivatives, including cationic skeletal rearrangements and reduction reactions with lanthanide salt additives.

AB - © 2016 Elsevier LtdA new clerodane was isolated from Dodonaea ceratocarpa and obtained in appreciable quantities (0.5% w/w plant). A variety of reactions on this clerodane provided access to a range of new derivatives, including cationic skeletal rearrangements and reduction reactions with lanthanide salt additives.

U2 - 10.1016/j.tet.2016.09.062

DO - 10.1016/j.tet.2016.09.062

M3 - Article

SN - 0040-4020

VL - 72

SP - 7470

EP - 7480

JO - Tetrahedron

JF - Tetrahedron

IS - 47

ER -

Isolation and chemistry of clerodane diterpenes from Dodonaea ceratocarpa

Abstract

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