Two new dimeric indole alkaloids from Tabernaemontana subglobosa MERR. from Taiwan

DOI: 10.1248/cpb.42.280

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 280 - 284 (1994)

Update date:2022-08-04

Topics:

Authors:

Takayama

Suda Suda

Chen Chen

Kitajima

Aimi Aimi

Sakai Sakai

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1248/cpb.42.280

The structures of two new bis-indole alkaloids, 19'(R)-hydroxyconodurine (11) and 19'(R)-hydroxyconoduramine (12), from the leaves of Tabernaemontana subglobosa MERR. (Apocynaceae), native to Taiwan, were determined by means of spectroscopic analysis and chemical reactions.

Full text of DOI:10.1248/cpb.42.280

NII-Electronic Library Service

Products guided by the article

Product name:methyl 13-methoxyibogamine-18-carboxylate

Cas No:596-54-3

R&D Labs maybe for 596-54-3

Rudong Zhenfeng Yiyang Chemical Co., Ltd.

Contact:0513-84573047

Address:South Fengli Town, Rudong County, Jiangsu Province, China
zhenjiang runjing high purity chemical co ltd

Contact:+86-511-83361155

Address:No.8.haixi road,international chemical park
Hunan Hui Bai Shi（YUNBANG）Biological Technology Co.,Ltd

website:http://www.hunanyunbang.com/

Contact:+86-731-85525605/+86-13319518603

Address:1103,C3 Building,No.27 Wenxuan Road, Yuelu District
GUANGZHOU MEDCAN PHARMATECH LTD

website:http://www.gzmedcan.com

Contact:+86-20-82519649

Address:Building J,Room 101,1 JiangtashanRd,Guang Zhou Science City,Guang Zhou ,China
Wuhan Silworld Chemical Co.,Ltd

website:http://www.silworldchemical.com

Contact:+86-27-85613400

Address:No.198 jiangjun Road, Wuhan,China 430033

Relevant to this article

Doi:10.1016/S0040-4039(00)91285-1
(1975)
Chemistry of Organo Halogenic Molecules. 140. Role of the Reagent Structure on the Transformations of Hydroxy Substituted Organic Molecules with the N-Fluoro Class of Fluorinating Reagents

Doi:10.1246/bcsj.68.1655
(1995)
Doi:10.1002/ardp.19763090510
(1976)
Radical OfC transposition: A metal-free process for conversion of phenols into benzoates and benzamides

Doi:10.1021/jo102467j
(2011)
Electrospray mass spectrometric investigation of the reactivity of the sulfide centers in [Pt₂(μ-S)₂(PPh₃) ₄] towards organic dihalides and the catalytic potential of this complex in the syntheses of organosulfu

Doi:10.1016/S1381-1169(03)00308-X
(2003)
A new type of acyclic, achiral nucleoside analogue. How does it simulate nucleosides?

Doi:10.1081/NCN-120022621
(2003)

Article Doi