Literature

Abstract

The 100 MHz p.m.r. data on the new ergot alkaloids agroclavine-I and epoxyagroclavine-I, metabolites of fungus Penicillium kapuscinskii strain UCM F-2156D, are reported. Their C and D rings are shown to exist in an "envelope" form. A cis orientation of the C/D ring junction is confirmed for both alkaloids. © 1984.

DOI： 10.1016/S0040-4039(01)91162-1

The conformational study of the new ergot alkaloids agroclavine-I and epoxyagroclavine-I by proton magnetic resonance spectroscopy

Tetrahedron Letters 1984.0

Researches on Ergot Fungus

Journal of the agricultural chemical society of Japan 1949.0

1-Methoxy-agroclavine from Penicillium sp. WC75209, a novel inhibitor of the Lck tyrosine kinase

Bioorganic & Medicinal Chemistry Letters 1998.0

Ergogaline, a new ergot alkaloid, produced by Claviceps purpurea: isolation, identification, crystal structure and molecular conformation

J. Chem. Soc., Perkin Trans. 2 2004.0

1-Methoxy-agroclavine from Penicillium sp. WC75209, a novel inhibitor of the Lck tyrosine kinase

Bioorganic & Medicinal Chemistry Letters 1998.0

New Alkaloids of Claviceps paspali