New Route to (+/-)-Magydardienediol, a Diterpene Isolated from Magydaris panacifolia (Vahl) Lange, via a Sequential Intra- and Inter-Molecular Radical C-C Bond-Forming Reaction

DOI: 10.1039/P19910001291

Source and publish data:

Journal of the Chemical Society. Perkin transactions I p. 1291 - 1295 (1991)

Update date:2022-08-05

Topics:

Authors:

Nagano, Hajime

Seko, Yuko

Nakai, Kyoko

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

Article abstract of DOI:10.1039/P19910001291

(+/-)-1-epi-Magydardienediol, and intermediate for the synthesis of (+/-)-magydardienediol and (+/-)-magydartrienol, diterpenes isolated from magydaris panacifolia (Vahl) Lange, has been synthesized stereoselectively from 3-methylcyclohex-2-enone in 12 st

Full text of DOI:10.1039/P19910001291

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:(4aS,7R,8S,8aS)-7-Methyl-8-(3-methyl-but-2-enyl)-7-(4-methyl-pent-3-enyl)-hexahydro-benzo[1,3]dioxine

Cas No:135404-74-9

R&D Labs maybe for 135404-74-9

KindChem Co.,Ltd,

Contact:+86-25-85281586

Address:13F,Bld2#,South of Longpan Road
Shanghai Bocimed Pharmaceutical Co., Ltd.

website:http://www.bocimed.com

Contact:+86-21-68861632

Address:Building 1, Lane 647, Songtao Road, Zhangjiang High-Tech Park, Shanghai
ZHUHAI HAIRUIDE BIOSCIENCE AND TECHNOLOGY CO.,LTD

website:http://www.zhhairuide.com

Contact:+8613326687259/+86-756-7789199

Address:No.10 Yonghui Road
WUHU HUAHAI BIOLOGY ENGINEERING CO LTD

Contact:+86-553-3836920

Address:7/F NO.82 LAODONG ROAD WUHU CHINA
CHINA MEHECO CORPORATION

Contact:+86-10-67147360/67107388

Address:No.18 Guangming Zhongjie, Chongwen District, Beijing, 100061, China

Relevant to this article

Synthesis and antidepressant-like activity of selenophenes obtained via iron(iii)-PhSeSePh-mediated cyclization of Z-selenoenynes

Doi:10.1039/c1ob06548c
(2012)
Enantioselective Total Synthesis of Nitraria Alkaloids: (+)-Nitramine, (+)-Isonitramine, (-)-Isonitramine, and (-)-Sibirine via Asymmetric Phase-Transfer Catalytic α-Allylations of α-Carboxylactams

Doi:10.1021/acs.joc.0c02573
(2021)
Remote stereocontrol in [3,3]-sigmatropic rearrangements: Application to the total synthesis of the immunosuppressant mycestericin G

Doi:10.1021/ol203300k
(2012)
Stereocontrolled total synthesis of fucoxanthin and its polyene chain-modified derivative

Doi:10.1021/ol203344c
(2012)
Multistep flow synthesis of vinyl azides and their use in the copper-catalyzed huisgen-type cycloaddition under inductive-heating conditions

Doi:10.3762/bjoc.7.168
(2011)
Taxol Structure-Activity Relationships: Synthesis and Biological Evaluation of 10-Deoxytaxol

Doi:10.1021/jo00063a001
(1993)

Article Doi