OCCURENCE OF EPIJUVABIONE-TYPE SESQUITERPENOIDS IN ABIES SACHALINENSIS

DOI: 10.1016/S0031-9422(00)97525-3

Source and publish data:

Phytochemistry p. 3773 - 3780 (1992)

Update date:2022-08-04

Topics:

Authors:

Numata, Atsushi

Kawai, Kenzo

Takahashi, Chika

Miyamoto, Tamie

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

Article abstract of DOI:10.1016/S0031-9422(00)97525-3

The wood of Abies sachalinensis from the Taisetsu mountain range of Japan afforded, in addition to 10 known compounds, seven new epijuvabione-type sesquiterpenoids, (+)-4'-dehydro-oxoepijuvabione, (-)-4'-dehydro-oxojuvabione, epijuvabienol ether, 5'-hydroxyepijuvabione, ar-dihydroxyepijuvabione, 3'-dehydroepijuvabi-5'-ol and 3'-isodihydroepitodomatuic acid.Their stereostructures were elucidated by chemical and spectral evidence. Key Word Index: Abies sachalinensis; Pinaceae; wood; epijuvabione anlogue; sesquiterpenoid.

Full text of DOI:10.1016/S0031-9422(00)97525-3

Products guided by the article

Product name:(+)-4'-dehydrooxojuvabione

Cas No:145075-77-0

R&D Labs maybe for 145075-77-0

NEWSTAR CHEM ENTERPRISE LTD.

Contact:0572-2722882

Address:1201,F3,xinghuibandao,
TaizhouTyloo Biopharm Co.,Ltd

website:http://www.tyloopharm.com

Contact:86-576-88785961

Address:No.529 ,Building B ,Junyuedasha Jiaojiang Zone
Tianjin Ji Ping Jia Chemical Co., Ltd.

Contact:18622448868

Address:tianjin
Borun Chemical Co.,Ltd.

Contact:+86-574- 87178138; 87297407

Address:No. 809, Liudingxingzuo, cangsong road, Ningbo, China
Debye Scientific

website:http://www.debyesci.com

Contact:+85221376140

Address:Rm. 19C, Lockhart Ctr., 301-307 Lockhart Rd., Wan Chai

Relevant to this article

A New Ring Transformation: Conversion of 6-p-Chlorophenyl-3-methyl-5-nitrosoimidazo<2,1-b>thiazole into 8-p-Chlorophenyl-8-hydroxy-5-methyl-3-oxo-1,2,4-oxadiazolo<3,4-c><1,4>thiazine by the Action of Mineral Acids

Doi:10.1039/c39920001394
(1992)
Triplex-forming ability of oligonucleotides containing 1-aryl-1,2,3- triazole nucleobases linked via a two atom-length spacer

Doi:10.1016/j.bmc.2013.05.034
(2013)
Acyclic butyl nucleic acid (BuNA): A novel scaffold for A-switch

Doi:10.1039/c3ra41255e
(2013)
Transition-metal-free catalyzed [3+2] cycloadditions/oxidative aromatization reactions for the synthesis of annulated indolizines

Doi:10.1039/c9nj03076j
(2019)
Asymmetric dihydroxylation route to a dipeptide isostere of a protease inhibitor: Enantioselective synthesis of the core unit of ritonavir

Doi:10.1039/a902518i
(1999)
Redox switching of conjugation length using 9,9,10,10-tetraaryl-9,10- dihydrophenanthrene as an ON/OFF unit: Preparation, x-ray structure, and redox properties of perfluorobiphenyl derivative and its S_nAr reactions to φextended analogues

Doi:10.1246/cl.130190
(2013)

Article Doi