MONOTERPENE ALKALOIDS FROM INCARVILLEA-SINENSIS .6. ABSOLUTE STEREOCHEMISTRY OF INCARVILLINE AND STRUCTURE OF A NEW ALKALOID, HYDROXYINCARVILLINE

Authors
CHI YM HASHIMOTO F YAN WM NOHARA T YAMASHITA M MARUBAYASHI N
Citation
Ym. Chi et al., MONOTERPENE ALKALOIDS FROM INCARVILLEA-SINENSIS .6. ABSOLUTE STEREOCHEMISTRY OF INCARVILLINE AND STRUCTURE OF A NEW ALKALOID, HYDROXYINCARVILLINE, Chemical and Pharmaceutical Bulletin, 45(3), 1997, pp. 495-498
Citations number
9
Categorie Soggetti
Pharmacology & Pharmacy",Chemistry
Journal title
Chemical and Pharmaceutical Bulletin → ACNP
ISSN journal
00092363
Volume
45
Issue
3
Year of publication
1997
Pages
495 - 498
Database
ISI
SICI code
0009-2363(1997)45:3<495:MAFI.A>2.0.ZU;2-3
Abstract
The absolute configuration of incarvilline (1), an important core comp ound of a number of alkaloids isolated from Incarvillea sinensis LAM., has been determined by the application of Mosher's method and X-ray c rystallographic analysis of incarvilline methiodide (1a). Furthermore, the structure of hydroxyincarvilline (2) was also determined by spect roscopic means.