Synthetic study on gymnodimine: Highly stereoselective construction of substituted tetrahydrofuran and cyclohexene moieties

DOI: 10.1055/s-1997-1075

Source and publish data:

Synlett p. 1417 - 1419 (1997)

Update date:2022-09-26

Topics:

Authors:

Ishihara, Jun

Miyakawa, Jun

Tsujimoto, Takashi

Murai, Akio

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

Article abstract of DOI:10.1055/s-1997-1075

The synthetic studies on gymnodimine, a shellfish toxin, are described. This marine toxin consists of 16-membered carbocycle, tetrahydrofuran, and spiro-imine moieties. Our synthetic strategy involves the stereoselective allylation of tetrahydrofuran compound and the exo-selective intramolecular Diels-Alder reaction.

Full text of DOI:10.1055/s-1997-1075

Products guided by the article

Product name:(E)-5-(4-Methoxy-benzyloxy)-3-methyl-pent-3-en-2-one

Cas No:1026879-50-4

R&D Labs maybe for 1026879-50-4

Henan zhongda Biological Engineering Co., Ltd

Contact:86-28-18109029985

Address:shenzhou road,xuedian industrial estate,zhengzhou city,henan province CHN
Synchemie Co., Ltd.

website:http://www.synchemie.com/

Contact:+86-574-87642758

Address:Room 901, Yinyi Bund Building， 132 Renmin Road
SuZhou LaiTeou

Contact:+86-0512-88957371

Address:shanghai
SuZhou Bichal Biological Technology CO.,LTD

Contact:+86-512-68051130

Address:NO.32 huoju road HI-TECH Industrial development zone SuZhou China
Suzhou JMS Chemical Co., Ltd.

Contact:+86-15995924277

Address:WuZhongOu suzhou new south road 89

Relevant to this article

Gas chromatography/mass spectrometry analysis of reaction products of sulfur mustards with phenol

Doi:10.1177/1469066719886424
(2020)
Quantitative structure-activity relationship modeling of dopamine D₁ antagonists using comparative molecular field analysis, genetic algorithms- partial least-squares, and K nearest neighbor methods

Doi:10.1021/jm980415j
(1999)
PtCl₂-catalyzed [6+2] cycloaddition of alkynes tethered to cycloheptatriene

Doi:10.1002/anie.200705482
(2008)
Enantioselective conjugate addition of aliphatic thiols to divergently activated electron poor alkenes and dienes

Doi:10.1016/j.tet.2014.06.035
(2014)
A General, Regiospecific Synthesis of Highly Substituted Quinones

Doi:10.1021/jo00365a043
(1986)
Dioxygenation of Long-Chain Alkadien(trien)ylphenols by Soybean Lipoxygenase

Doi:10.1021/jf980196a
(1998)

Article Doi