Stereochemistry of the dibenzopyrrocoline alkaloids cryptaustoline and cryptowoline

Seiichi Takano; Shigeki Satoh; Yoshiteru Oshima; Kunio Ogasawara

doi:10.3987/R-1987-06-1487

Stereochemistry of the dibenzopyrrocoline alkaloids cryptaustoline and cryptowoline

Seiichi Takano, Shigeki Satoh, Yoshiteru Oshima, Kunio Ogasawara

PHA - Molecular Pharmaceutical Science

Research output: Contribution to journal › Article › peer-review

5 Citations (Scopus)

Abstract

Stereochemistry of the dibenzopyrrocoline alkaloids, (-)-cryptaustoline (1) and (-)-cryptowoline (2), isolated from the Australian shrub Cryptocaria bowiei is deduced both as 7R, 13S configuration with cis B C ring structure based on the analysis of proton-nmr spectra of synthetic materials.

Original language	English
Pages (from-to)	1487-1489
Number of pages	3
Journal	Heterocycles
Volume	26
Issue number	6
DOIs	https://doi.org/10.3987/R-1987-06-1487
Publication status	Published - 1987 Jun 1

ASJC Scopus subject areas

Analytical Chemistry
Pharmacology
Organic Chemistry

Access to Document

10.3987/R-1987-06-1487

Cite this

@article{c9fc6452c9954fcc9b4586cf9f9e716d,

title = "Stereochemistry of the dibenzopyrrocoline alkaloids cryptaustoline and cryptowoline",

abstract = "Stereochemistry of the dibenzopyrrocoline alkaloids, (-)-cryptaustoline (1) and (-)-cryptowoline (2), isolated from the Australian shrub Cryptocaria bowiei is deduced both as 7R, 13S configuration with cis B C ring structure based on the analysis of proton-nmr spectra of synthetic materials.",

author = "Seiichi Takano and Shigeki Satoh and Yoshiteru Oshima and Kunio Ogasawara",

year = "1987",

month = jun,

day = "1",

doi = "10.3987/R-1987-06-1487",

language = "English",

volume = "26",

pages = "1487--1489",

journal = "Heterocycles",

issn = "0385-5414",

publisher = "Japan Institute of Heterocyclic Chemistry",

number = "6",

}

TY - JOUR

T1 - Stereochemistry of the dibenzopyrrocoline alkaloids cryptaustoline and cryptowoline

AU - Takano, Seiichi

AU - Satoh, Shigeki

AU - Oshima, Yoshiteru

AU - Ogasawara, Kunio

PY - 1987/6/1

Y1 - 1987/6/1

N2 - Stereochemistry of the dibenzopyrrocoline alkaloids, (-)-cryptaustoline (1) and (-)-cryptowoline (2), isolated from the Australian shrub Cryptocaria bowiei is deduced both as 7R, 13S configuration with cis B C ring structure based on the analysis of proton-nmr spectra of synthetic materials.

AB - Stereochemistry of the dibenzopyrrocoline alkaloids, (-)-cryptaustoline (1) and (-)-cryptowoline (2), isolated from the Australian shrub Cryptocaria bowiei is deduced both as 7R, 13S configuration with cis B C ring structure based on the analysis of proton-nmr spectra of synthetic materials.

UR - http://www.scopus.com/inward/record.url?scp=12644278526&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=12644278526&partnerID=8YFLogxK

U2 - 10.3987/R-1987-06-1487

DO - 10.3987/R-1987-06-1487

M3 - Article

AN - SCOPUS:12644278526

SN - 0385-5414

VL - 26

SP - 1487

EP - 1489

JO - Heterocycles

JF - Heterocycles

IS - 6

ER -

Stereochemistry of the dibenzopyrrocoline alkaloids cryptaustoline and cryptowoline

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this