CYCLIZATION, AROMATIZATION AND EXPULSION REACTIONS OF BETA-CAROTENE DURING SEDIMENT DIAGENESIS

Citation
Jss. Damste et al., CYCLIZATION, AROMATIZATION AND EXPULSION REACTIONS OF BETA-CAROTENE DURING SEDIMENT DIAGENESIS, Tetrahedron letters, 38(13), 1997, pp. 2347-2350
Citations number
11
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00404039
Volume
38
Issue
13
Year of publication
1997
Pages
2347 - 2350
Database
ISI
SICI code
0040-4039(1997)38:13<2347:CAAERO>2.0.ZU;2-J
Abstract
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.