Autoxidation of 4-amorphen-11-ol and the biogenesis of nor- and seco-amorphane sesquiterpenes from Fabiana imbricata

DOI: 10.1016/S0040-4020(99)00986-2

Source and publish data:

Tetrahedron p. 15109 - 15126 (1999)

Update date:2022-07-30

Topics:

Authors:

Ngo, Koon-Sin

Brown, Geoffrey D.

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

Article abstract of DOI:10.1016/S0040-4020(99)00986-2

Photooxidation of 4-amorphen-11-ol (1), recently reported as one of the major sesquiterpene natural products from the medicinal plant Fabiana imbricata, results in three allylic hydroperoxides 6, 9 and 10, which are expected from the 'ene- type' reaction

Full text of DOI:10.1016/S0040-4020(99)00986-2

Products guided by the article

Product name:4-((3aR,4S,5R,7aS)-3a-Hydroperoxy-3-hydroxy-1,1,5-trimethyl-octahydro-isobenzofuran-4-yl)-butan-2-one

Cas No:256643-45-5

R&D Labs maybe for 256643-45-5

Chengdu Chengnuo New-Tech Co., Ltd

Contact:0086-028-85749078

Address:4 Jiuyang road,Jiulong industrial port,Chengdu, China
changsha chenjin chemical technology co.,LtD(expird)

Contact:86-731-84451263

Address:Room 201/217-218, 101 Jingyuan Electronic Technology Co.,Ltd. Testing Center, No.69, Lufeng Road, High-tech Development Zone, Changsha, China
Shandong united-rising pharmaceutical cooperation.,ltd.

Contact:008653187965009

Address:171No., Jing5 Road, Shizhong District, Jinan, China
Jiangsu Hualun Chemical Industry Co., Ltd

website:http://www.hualunchem.com

Contact:+86-0514-86464168 86507985

Address:39# Middle Renmin Road, Dinghuo Town
Fujian Wanke Pharmaceutical Co., LTD.

Contact:+86-598-5026002

Address:Economic development zone,jiangle county

Relevant to this article

The cleavage of meso-epoxides with homochiral thiols: Synthesis of (+)- and (-)-trans-1-mercaptocyclohexan-2-ol

Doi:10.1016/S0957-4166(99)00446-2
(1999)
Diastereoselective photocycloaddition of an axial chiral enamide

Doi:10.1016/S0040-4039(99)01933-4
(1999)
Doi:10.1021/jm00297a050
(1970)
Captodative olefin 3-p-nitrobenzoyloxy-3-buten-2-one as a Diels-Alder ketene equivalent for the synthesis of γ-hydroxycyclohexenones

Doi:10.1016/S0040-4020(99)00928-X
(1999)
Doi:10.1016/S0040-4039(01)88670-6
(1969)
A short synthesis of the β-amyloid (Aβ) aggregation inhibitor 3-p-toluoyl-2-[4'-(3-diethylaminopropoxy)-phenyl]-benzofuran.

Doi:10.1016/S0040-4039(99)02030-4
(1999)

Article Doi