Total Synthesis of (+/-)-12-Hydroxy-5(Z),8(Z),10(E),14(Z)-eicosatetraenoic Acid (12-HETE)

DOI: 10.1021/jo00222a054

Source and publish data:

Journal of Organic Chemistry p. 4417 - 4418 (1985)

Update date:2022-08-03

Topics:

Authors:

Gunn, Bruce P.

Brooks, Dee W.

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

Article abstract of DOI:10.1021/jo00222a054

A total synthesis of 12-HETE is reported which incorporates an oxidative cleavage of an appropriately substituted furan to provide a functionalized trans-allylhydroxy fragment which is subsequently elaborated in an operationally simple manner affording a practical preparation of 12-HETE.

Full text of DOI:10.1021/jo00222a054

Products guided by the article

Product name:2,6-Dodecadienal, 4-hydroxy-, (2E,6Z)-

Cas No:126254-48-6

R&D Labs maybe for 126254-48-6

Hongyi Import & Export CO.,LTD

Contact:86-13319649499

Address:Nanzheng Neighborhood Commitees, Chongwen Office, Yongding District
Rugao Jinling Chemical Co., Ltd.(expird)

Contact:0086-513-68005586

Address:Lianluo new village huangshi town Rugao city Jiangsu Province.
China Synchem Technology Co.,Ltd

website:http://www.cnsynchem.com

Contact:+86-0552-4929311

Address:No.217 Daqing Road
Shanghai Harvest Chemical Ind. Co., Ltd.

Contact:021-51385350

Address:ROOM 806-807, AI LI CHEN BUILDING, No.333 JINGXIANG ROAD, PUDONG DISTRICT, 201206, SHANGHAI
shanghai payne pharm co.,ltd.

Contact:+86-021-58123769

Address:No.780 of Cailun Road,Zhangjiang Hi-tech Park,Pudong,Shanghai

Relevant to this article

Doi:10.1016/S0040-4020(01)91723-5
(1971)
Addition reactions to chiral aziridine-2-carboxaldimine toward various enantiopure nitrogen-containing heterocycles

Doi:10.1016/j.tet.2005.07.064
(2005)
Preparation of optically active α-hydroxy oxime ether by diastereoselective imino 1,2-Wittig rearrangement of hydroximates and its application to synthesis of (+)-cytoxazone

Doi:10.1016/j.tetlet.2005.04.026
(2005)
Triazine based bipolar host materials for blue phosphorescent OLEDs

Doi:10.1021/cm4023216
(2013)
Doi:10.1002/ardp.19422800702
(1942)
Ambident reactivity of the nitrite ion revisited

Doi:10.1002/anie.200501274
(2005)

Article Doi