Synthesis and absolute configuration of stellettadine A: A marine alkaloidthat induces larval metamorphosis in ascidians

Authors
Nozawa, D Takikawa, H Mori, K
Citation
D. Nozawa et al., Synthesis and absolute configuration of stellettadine A: A marine alkaloidthat induces larval metamorphosis in ascidians, BIOORG MED, 11(12), 2001, pp. 1481-1483
Citations number
16
Categorie Soggetti
Chemistry & Analysis
Journal title
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
ISSN journal
0960894X → ACNP
Volume
11
Issue
12
Year of publication
2001
Pages
1481 - 1483
Database
ISI
SICI code
0960-894X(20010618)11:12<1481:SAACOS>2.0.ZU;2-J
Abstract
Stelletradine A, a bisguanidinium alkaloid isolated from a marine sponge St elletta sp. as an inducer of larval metamorphosis in ascidians, and its unn atural enantiomer were synthesized from the enantiomers of citronellal. The absolute configuration of stellettadine A was established as R. (C) 2001 E lsevier Science Ltd. All rights reserved.