Jss. Damste et al., CYCLIZATION, AROMATIZATION AND EXPULSION REACTIONS OF BETA-CAROTENE DURING SEDIMENT DIAGENESIS, Tetrahedron letters, 38(13), 1997, pp. 2347-2350
A novel diaryl isoprenoid 1 with an additional aromatic ring (C30H38),
formed from the carotenoid beta-carotene by cyclisation, aromatisatio
n and expulsion reactions during sediment diagenesis, has been isolate
d from a 50 Ma old lacustrine sedimentary rock and identified by H-1 a
nd C-13 NMR spectroscopy and mass spectrometry. (C) 1997 Elsevier Scie
nce Ltd.