Ultrasound in Organic Synthesis. 18. Selective Oxymercuration via Sonochemically in Situ Generated Mercury Salts

DOI: 10.1021/jo00280a001

Source and publish data:

Journal of Organic Chemistry p. 4479 - 4481 (1989)

Update date:2022-08-31

Topics:

Authors:

Einhorn, J.

Einhorn, C.

Luche, J. L.

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

Article abstract of DOI:10.1021/jo00280a001

Selective mercuration of diolefins is favored by a proper choice of the mercuric salt, which can be generated in situ from mercuric oxide and the corresponding acid under sonochemical activation.

Full text of DOI:10.1021/jo00280a001

Products guided by the article

Product name:(±)-α,α,4-trimethylcyclohex-3-ene-1-methanol

Cas No:2438-12-2

R&D Labs maybe for 2438-12-2

JiangXi Hong Run Chemical Co., Ltd

Contact:+86-0791-88521351

Address:XingHuo industrial zone in YongXiu county
QINGDAO NEW FLOURISH INTERNATIOANAL TRADE CO., LTD.

Contact:+86 532 80861829

Address:No. 1, Yinchuan East Road, 266061, Qingdao, China
HANGZHOU FOREWIN PHARMA CO., LTD

Contact:+86-571-89053961

Address:hangzhou
Dalian Join King Biochemical Tech. Co., Ltd.

Contact:0411 39216206

Address:814 First State Blvd
Disynthesis Chemical Technology Co. Ltd.

Contact:+86-571-88194596

Address:Dengyun road 380, Gongshu district, Hangzhou city, China

Relevant to this article

Solvophobic control of core-substituted naphthalene diimide nanostructures

Doi:10.1039/b920015k
(2010)
Doi:10.1039/c29700000972
(1970)
Doi:10.1021/ja01158a025
(1950)
Copper-Catalyzed Aerobic Oxidative C(aryl)-OH Bond Functionalization of Catechols with Amines Affording Benzoxazoles

Doi:10.1002/adsc.201500515
(2015)
Doi:10.1246/bcsj.43.3924
(1970)
Doi:10.1016/S0040-4020(01)98078-0
(1971)

Article Doi