Jump to main content
Jump to site search
PLANNED MAINTENANCE Close the message box

Scheduled maintenance work on Wednesday 22nd May 2019 from 11:00 AM to 1:00 PM (GMT).

During this time our website performance may be temporarily affected. We apologise for any inconvenience this might cause and thank you for your patience.


Issue 3, 1972
Previous Article Next Article

Structures of the natural products blumenols A, B, and C

Abstract

Blumenols A, B, and C, new compounds from Podocarpus blumei, are shown to have structures (1), (2), and (3), respectively, with the opposite stereochemistry to that of abscisic acid (4) at the ring chiral centre.

Back to tab navigation

Article type: Paper
DOI: 10.1039/C39720000113
J. Chem. Soc., Chem. Commun., 1972, 113-114

  •   Request permissions

    Structures of the natural products blumenols A, B, and C

    M. N. Galbraith and D. H. S. Horn, J. Chem. Soc., Chem. Commun., 1972, 113
    DOI: 10.1039/C39720000113

Search articles by author

Spotlight

Advertisements