A QUINONE METHIDE DITERPENOID FROM THE ROOT OF SALVIA MOORCRAFTIANA

DOI: 10.1016/0031-9422(86)88043-8

Source and publish data:

Phytochemistry p. 755 - 756 (1986)

Update date:2022-08-11

Topics:

Authors:

Simoes, Fatima

Michavila, Antonio

Rodriguez, Benjamin

Garcia-Alvarez, Maria C.

Hasan, Mashooda

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

Article abstract of DOI:10.1016/0031-9422(86)88043-8

A new diterpenic methylenquinone, 15-deoxyfuerstione, was isolated from the root of Salvia moorcraftiana.The structure of this natural compound was established by chemical and spectroscopic means to be 11-hydroxy-5,7,9(11),13-abietatetraen-12-one.The previously known diterpenoids 7α-acetoxyroyleanone and taxodione were also found in the same source.Key Word Index - Salvia mmoorcraftiana; Labiatae; diterpenoids; abietane derivatives; 15-deoxyfuerstione; 7α-acetoxyroyleanone; taxodione.

Full text of DOI:10.1016/0031-9422(86)88043-8

Products guided by the article

Product name:Saprorthoquinone

Cas No:102607-41-0

R&D Labs maybe for 102607-41-0

Jiangxi Dongxu Chemical Science & Technology Co.,Ltd

Contact:+86-791-86899381

Address:Nanchang, Jiangxi, China
Nanjing yieldpharma co.ltd

Contact:13813902930 025-52714267

Address:20 Fengji Road, Yuhua Economic Development Zone, Nanjing, Jiangsu, P. R. China
ShangHai Soyoung Biotechnology Inc

website:http://www.soyoungbio.com

Contact:+86-21-69893009

Address:shanghai
Anhui Qingyun Pharmaceutical and Chemical Co.,Ltd

Contact:+86-551-63633067

Address:Shuangfeng Road Hefei Anhui
Suzhou Time-chem Technologies Co., Ltd.

Contact:0512-63983931/68086856

Address:No. 1326 of Binhe Road, New District, Suzhou, Jiangsu, P. R. China

Relevant to this article

Polymer-supported quenching reagents for parallel purification

Doi:10.1021/ja9634637
(1997)
Synthesis, structure and conformational properties of fluoroformylchlorodifluoroacetyl disulfide, FC(O)SSC(O)CF₂Cl: Conformational transferability in -C(O)SSC(O)- compounds

Doi:10.1002/ejic.200600604
(2006)
Effects of normal and their branched alcohols with structurally minimal variation on kinetic parameters in thermolysin-catalyzed peptide hydrolysis and synthesis of N-(benzyloxycarbonyl)-L-phenylalanyl-L-phenylalanine and its methyl ester.

Doi:10.1271/bbb.59.535
(1995)
THE ABSOLUTE STEREOCHEMISTRY OF THE ENZYMIC CYCLISATION TO FORM THE STERPURENE SESQUITERPENES

Doi:10.1016/S0040-4039(00)80491-8
(1988)
[2+2+2]-Cycloaddition of 4-Hydroxy-Substituted Enediynes to 2-Hydroxy-Substituted Decahydrophenanthrenes

Doi:10.1002/ejoc.200300432
(2003)
Carbon-13 NMR Spectra of 1,3-Dioxolanes. II - Determination of α, β and γ Parameters for 2- and 4-Methyl Groups in Stereoisomeric Derivatives by the Pattern Molecule Method

Doi:10.1002/mrc.1260260204
(1988)

Article Doi