TERPENOID AND FLAVONE CONSTITUENTS OF POLEMONIUM VISCOSUM

DOI: 10.1016/0031-9422(88)83132-7

Source and publish data:

Phytochemistry p. 517 - 522 (1988)

Update date:2022-08-02

Topics:

Authors:

Stierle, Donald B.

Stierle, Andrea A.

Larsen, R. D.

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

Article abstract of DOI:10.1016/0031-9422(88)83132-7

The chemical investigation of Polemonium viscosum yielded several new diterpenes with labdane and pimarane skeletons, a new flavone and two new monoterpene glycosides.The absolute configuration of akhardiol is established by X-ray structure determination of the O-bromobenzoate derivative.Key Word Index-Polemonium viscosum; Polemoniaceae; labdane diterpenes; flavone; monoterpene glycosides; 13C NMR investigation; X-ray structure.

Full text of DOI:10.1016/0031-9422(88)83132-7

Products guided by the article

Product name:4H-1-Benzopyran-4-one, 5-(acetyloxy)-6,7-dimethoxy-2-phenyl-

Cas No:94306-12-4

R&D Labs maybe for 94306-12-4

Compro Shijiazhuang Fine Chemical Co., Ltd

Contact:0086-311-89689838

Address:Economic and Technological Development Zone of Shijiazhuang,Hebei
ANHUI WEICHI CHEMICAL CO.,LTD

website:http://www.weichichem.com

Contact:+8613912949432

Address:Fine Chemical Industrial Base,Wujiang town,He County,Anhui China.
King Brother Chem Co., Ltd

website:http://www.uvchemkeys.com

Contact:0086-021-58785816

Address:RM2607 Building No.1 Guosheng, Lane 388, Zhongjiang Road, Putuo District, Shanghai 200062 China
Changzhou LanXu Chemical Co.,ltd.(expird)

Contact:86-0519-86330911,13656129734,15261186386

Address:Room 524, Depart.Chemical, Changzhou Science and Eductaion town, Jiangsu, China;Factory: Haian Fine Chemical Industry Park,Nantong,Jiangsu,China
SHANGHAI RC CHEMICALS CO.,LTD.

website:http://www.rcc.net.cn

Contact:+86-21-50322175

Address:Rm1415 Yinqiao Masion No.58 Jinxin Road Pudong Shanghai China

Relevant to this article

Studies of zoanthamine alkaloids. Enantiocontrolled construction of the tetracyclic hemi-aminal core

Doi:10.1016/S0040-4039(98)00369-4
(1998)
Facile Synthesis of β-Aryl- or β-Alkenyl-β-methyl-α,β-unsaturated Carbonyl Compounds by Palladium-Catalyzed Reaction of 1,2-Dien-4-ols with Aryl or Alkenyl Halides.

Doi:10.1021/jo00204a024
(1985)
Selective reduction of ortho-Acylatedβ-enaminones of homoveratryamine and their cyclization to 1,2,3,4-tetrahydroisoquinolines withβ-enaminone moiety

Doi:10.1080/00397911.2011.589020
(2013)
Direct Displacement with Anhydrous Fluoride of the C-2 Trifluoromethanesulfonate of Methyl 4,6-O-Benzylidene-3-O-methyl-2-O-trifluoromethylsulfonyl-β-D-mannopyranoside

Doi:10.1039/c39820000972
(1982)
Synthesis of 1,3-Oxazine-4-thione Derivatives through an Efficient, Rapid and Green Method Catalyzed by L-Proline in Aqueous Medium

Doi:10.1080/00304948.2018.1468984
(2018)
Synthesis, biological evaluation and docking studies of novel benzopyranone congeners for their expected activity as anti-inflammatory, analgesic and antipyretic agents

Doi:10.1016/j.bmc.2009.05.073
(2009)

Article Doi