Stereochemistry of cis-clerodane diterpenes
Abstract
null null To piscicidal solidagolactones [IV, V, VII and VIII (1~4, null null null cis null null -clerodane diterpenes)] isolated from null null null Solidago null null null null null null altissima null null , a non-steroidal conformation was assigned on the basis of chemical and physicocheaical evidence. 13C NMR chemical shifts of methyl groups proved useful for determining stereochemistry of the A/B ring junction in clerodanes. For clerodanes...
Paper Details
Title
Stereochemistry of cis-clerodane diterpenes
Published Date
Jan 1, 1986
Journal
Volume
42
Issue
13
Pages
3461 - 3470
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