13C NMR Data for Labdane Diterpenoids

DOI: 10.1002/mrc.1260310317

Source and publish data:

Magnetic Resonance in Chemistry p. 299 - 308 (1993)

Update date:2022-09-26

Topics:

Authors:

Barrero, Alejandro F.

Altarejos, Joaquin

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

Article abstract of DOI:10.1002/mrc.1260310317

The analysis of the 13C NMR spectra of 91 labdane-type compounds, classified into ten different series, is reported. KEY WORDS: 13C NMR, Diterpenes, Labdanes, Substituted trans-decalins, 2D NMR

Full text of DOI:10.1002/mrc.1260310317

Products guided by the article

Product name:Methyl (8R,13R)-8,13-epoxylabdan-19-oate

Cas No:138662-83-6

R&D Labs maybe for 138662-83-6

Jurong Huaheng Natural Biological Products Factory

website:http://www.risebiochem.com

Contact:+86-13921007726

Address:Chuncheng town,Jurong city,Jiangsu province,China
taizhou creating bio-pharm co.,ltd.

Contact:+86- 576- 88827176

Address:715 room ,unit A.junyue Building,Jiaojiang,Taizhou,Zhejiang,China
Qingdao Kingway Pharmtech Co., Ltd.

Contact:86-532-87118899

Address:No. 88, Middle Haixi Road, Jiaonan City, Qingdao, China
Daqing New Century Fine Chemical Co., Ltd.(expird)

Contact:010-57126694

Address:No.39, jinxing cun, honggang district
Nanjing Legend Pharmaceutical & Chemical Co., Ltd.

Contact:+86-25-83767696

Address:14-7 Zhongshan Lu Guluo District, Nanjing

Relevant to this article

On the ingredients of the green amanita. XXX. Structures of amanatines

Doi:10.1002/jlac.19667000119
(1966)
Synthesis and antitumor activity of novel 4-(2-fluorophenoxy)quinoline derivatives bearing the 4-Oxo-1,4-dihydroquinoline-3-carboxamide moiety

Doi:10.1002/ardp.201300029
(2013)
A catalyst free, one pot approach for the synthesis of quinoxaline derivatives via oxidative cyclisation of 1,2-diamines and phenacyl bromides

Doi:10.1016/j.tetlet.2015.01.138
(2015)
Visible light-induced photocatalytic C-H ethoxycarbonylmethylation of imidazoheterocycles with ethyl diazoacetate

Doi:10.1039/d0ra05795a
(2020)
Metabolic stability optimization and metabolite identification of 2,5-thiophene amide 17 β-hydroxysteroid dehydrogenase type 2 inhibitors

Doi:10.1016/j.ejmech.2014.09.061
(2014)
A highly fluorescent DNA toolkit: Synthesis and properties of oligonucleotides containing new Cy3, Cy5 and Cy3B monomers

Doi:10.1093/nar/gks303
(2012)

Article Doi