Studies on the syntheses of sesquiterpene lactones. III. Improved synthesis of vulgarin

DOI: 10.1246/bcsj.52.2737

Source and publish data:

Bulletin of the Chemical Society of Japan p. 2737 - 2738 (1979)

Update date:2022-08-03

Topics:

Authors:

Ando Ando

Tajima Tajima

Takase Takase

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

Article abstract of DOI:10.1246/bcsj.52.2737

Full text of DOI:10.1246/bcsj.52.2737

Products guided by the article

Product name:4-epi-vulgarin

Cas No:66289-87-0

R&D Labs maybe for 66289-87-0

Global United Biotechnology Inc.

Contact:+86-21-61618568

Address:Room 309, Building 6, NO.135, Jinyu Road, Pudong
Shandong Xinhua Pharmaceutical Co.,Ltd

website:http://www.xhzy.com

Contact:+86-533-2196801

Address:1 lutai road,zhangdian dis,Zibo City
ABA Chemicals (Shanghai) Limited

Contact:021- 5115 9199-232

Address:Suite 18D, #201 Ningxia Road,
China Synchem Technology Co.,Ltd

website:http://www.cnsynchem.com

Contact:+86-0552-4929311

Address:No.217 Daqing Road
Nanjing Fred Technology Co.,Ltd.

website:http://www.fredbio.com

Contact:+86-25-84696168

Address:Nanjing

Relevant to this article

Unified total syntheses of the inositol polyphosphates: D-I-3,5,6P ₃, D-I-3,4,5P₃, D-I-3,4,6P₃, and D-I-3,4,5,6P₄ via catalytic enantioselective and site-selective phosphorylation

Doi:10.1021/jo0610816
(2006)
Practical synthesis of Boc-protected cis-4-trifluoromethyl and cis-4-difluoromethyl-L- prolines

Doi:10.1021/jo0257400
(2002)
Chemical Synthesis of Side-Chain-Hydroxylated Vitamin D₃ Derivatives and Their Metabolism by CYP27B1

Doi:10.1002/cbic.202100250
(2021)
Synthesis and investigation of conformationally restricted analogues of lavendustin A as cytotoxic inhibitors of tubulin polymerization

Doi:10.1021/jm0202270
(2002)
An efficient method for synthesis of succinate-based MMP inhibitors

Doi:10.1021/ol026331t
(2002)
Solvent-Free Synthesis of Salen Ligands and Pd(II)- and Cu(II)-Salen Complexes: Their Use in the Oxidation of α-Tetralones to α-Naphthols

Doi:10.1055/s-0036-1588446
(2017)

Article Doi