Conformational studies and stereochemical assignments of the lactarane sesquiterpenes furoscrobiculin D and blennin D☆
Furoscrobiculin D and blennin D were assigned stereostructures 4 and 5, respectively, by molecular mechanics and 1H NMR spetroscopy.
References (12)
- et al.
Phytochemistry
(1980) - et al.
Tetrahedron
(1986) - et al.
Tetrahedron
(1993) - et al.
Tetrahedron
(1980) - et al.
Tetrahedron Lett.
(1985) - et al.
Tetrahedron Lett.
(1982)
There are more references available in the full text version of this article.
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Communication N. 31 of the series “Fungal metabolites”. For part 30 see Gamba-Invernizzi, A.; Garlaschelli, L.; Rossi, A.; Vidari, G.; Vita-Finzi, P. J. Nat. Prod. 1993, 56, 000.
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