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Chemistry of the Podocarpaceae. L. Conversion of 12-Hydroxypodocarpa-8,11,13-trien-19-oic acid (podocarpic acid) into 19-Hydroxypodocarp-8(14)-en-13-one

RC Cambie, RC Hayward and AW Missen
27(11) pp.2413 - 2420


5 articles found in Crossref database.

ChemInform Abstract: CHEMISTRY OF THE PODOCARPACEAE PART 50, CONVERSION OF 12‐HYDROXYPODOCARPA‐8,11,13‐TRIEN‐19‐OIC ACID (PODOCARPIC ACID) INTO 19‐HYDROXYPODOCARP‐8(14)‐EN‐13‐ONE
CAMBIE R. C., HAYWARD R. C., MISSEN A. W.
Chemischer Informationsdienst. 1975 6(7).
Synthesis of (−)-auricularic acid and its C-4 epimer the absolute configuration of auricularic acid
Abad Antonio, Arnó Manuel, Peiró Miguel, Zaragozá Ramon J.
Tetrahedron. 1991 47(23). p.3829
Organic Reactions (1993)
Krow Grant R.
Chemistry of the podocarpaceae
Cambie Richard C., Clark George R., Gallagher Stewart R., Rutledge Peter S., Stone Martin J., Woodgate Paul D.
Journal of Organometallic Chemistry. 1988 342(3). p.315
The neutral deoxygenation (reduction) of aryl carbonyl compounds with raney-nickel. an alternative to the clemmenson, wolf-kishner or mozingo (thioketal) reductions.
Mitchell Reginald H., Lai Yee-Hing
Tetrahedron Letters. 1980 21(27). p.2637

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