“…This synthetic work led to revision of the absolute configurations that had previously been assigned to mactraxanthin pared by a biomimetic route, involving concerted hydroxyprenylation-cyclization of a C, or C, acyclic precursor of the e n d -g r ~u p . ~~ Selective rearrangement of 5,6,5',6'-diepoxy-5,6,5',6'-tetrahydro-r),p-carotene (60) in diethyl ether that contained malonic acid gave a mixture of the 8'-epimeric luteoc hromes [ 5,6,5',8'-diepoxy-5,6,5', 8'tetrahydro-P,P-carotenes] (61) and (62). 40 The preparation of the pyridinium carotene analogue (63) as a potential antitumour agent has been de~cribed.~' Further work on the preparation and properties of carotenoporphyrin-quinone structures such as (67)…”