16-EPI-19-S-VINDOLININE, AN INDOLINE ALKALOID FROM CATHARANTHUS ROSEUS

DOI: 10.1016/0031-9422(83)85046-8

Source and publish data:

Phytochemistry p. 1021 - 1024 (1983)

Update date:2022-08-17

Topics:

Authors:

Atta-Ur-Rahman

Bashir, M.

Kaleem, S.

Fatima, T.

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

Article abstract of DOI:10.1016/0031-9422(83)85046-8

Key Word Index - Catharanthus roseus; Apocynaceae; leves; indole alkaloids; 13C NMR; 16-epi-19-S-vindolinine. Studies on the aslkaloids of Catharanthus roseus have resulted in the isolation of a new alkaloid, to which the structure of 16-epi-19-S-vindolinine has been assigned.

Full text of DOI:10.1016/0031-9422(83)85046-8

Products guided by the article

Product name:(21R)-(+)-vincadifformine

Cas No:15539-10-3

R&D Labs maybe for 15539-10-3

guide(suzhou) fine materials co. ltd

Contact:0512-80972173

Address:21st Building, No.369 Lushan Rd, New District Suzhou China 215129
Guangzhou Chemical Reagent Factory

Contact:+86-20-8435 9820 or 8435 7345

Address:Southern Guangzhou, Guangdong, China
Hubei Honch Pharmaceutical Co.,Ltd

Contact:86-713-7222018

Address:Li Shizhen Pharmaceutical Industry park, Qichun County, Hubei Province,China
Hawks Chemical

Contact:+44 (0)161 367 9441

Address:
Shanghai UCHEM Inc.

Contact:+86-21-56338808

Address:799 Dunhuang Road, Putuo

Relevant to this article

Doi:10.1093/oxfordjournals.jbchem.a128852
(1968)
Doi:10.1246/bcsj.12.8
(1937)
Use of dimethyl carbonate as a solvent greatly enhances the biaryl coupling of aryl iodides and organoboron reagents without adding any transition metal catalysts

Doi:10.1039/c2cc17401d
(2012)
Binuclear mercury(II) complexes of sulfonium ylides: Synthesis, structural characterization and anti-bacterial activity

Doi:10.1016/j.molstruc.2012.10.051
(2013)
UV cell stress induces oxidative cyclization of a protective reagent for DNA damage reduction in skin explants

Doi:10.1016/j.freeradbiomed.2018.12.037
(2019)
Iron(II) Induced Activation of Hydrogen Peroxide in Ferryl Ion (FeO²⁺) and Singlet Oxygen (1O2) in Acetonitrile: Monoxygenations, Dehydrogenations, and Dioxygenations of Organic Substrates

Doi:10.1021/ja00327a047
(1984)

Article Doi