Reaction of 2-Aryl-3-(N,N-dimethylamino)-1-propenes and Their Corresponding Quaternary Ammonium Salts with Organometallic Species and Reducing Agents

DOI: 10.1021/jo00392a035

Source and publish data:

Journal of Organic Chemistry p. 3683 - 3686 (1987)

Update date:2022-08-05

Topics:

Authors:

Gupton, John T.

Layman, William J.

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

Article abstract of DOI:10.1021/jo00392a035

A series of 2-aryl-3-(N,N-dimethylamino)-1-propenes and their corresponding quaternary ammonium salts were reacted with a variety of organometallic species and reducing agents.The utility of such reactions for the preparation of α-substituted styrene derivatives is discussed.

Full text of DOI:10.1021/jo00392a035

Products guided by the article

Product name:<2-(3,4-dimethoxyphenyl)prop-1-en-3-yl>trimethylammonium iodide

Cas No:109125-11-3

R&D Labs maybe for 109125-11-3

Taizhou YOJOY Chemical Co., Ltd.

Contact:13857143241

Address:Yangfu Industrial Park, Xianju, Zhejiang, P. R. China
Hunan Shineway Enterprise Co., Ltd.

Contact:+86-731-86303875

Address:118, Huanghua International Airport Road, Huanghua Town, Changsha, Hunan 410137, China
Chameleon Specialty Chemicals

Contact:+44 7958 511245

Address:PO Box 469, Manchester, UK
Chongqing maohuan Chemicals Co., Ltd

website:http://www.bschem.com

Contact:+86 13996103726

Address:Chongqing Nan'an District Tu Town
MedicalChem(Yancheng)Manuf.Co.,Ltd.

Contact:+86-515-84383366

Address:Touzeng BinHai, YanCheng City, JiangSu Province, China

Relevant to this article

Gold-catalyzed deoxygenative Nazarov cyclization of 2,4-dien-1-als for stereoselective synthesis of highly substituted cyclopentenes

Doi:10.1021/ja806415t
(2008)
Discovery and SAR of potent, orally available 2,8-diaryl-quinoxalines as a new class of JAK2 inhibitors

Doi:10.1016/j.bmcl.2010.02.056
(2010)
Stereoselective synthesis of branched cyclopentitols by titanium(III)-promoted reductive cyclization of 4-oxiranylaldehydes and 4-oxiranyl ketones derived from hexoses

Doi:10.1055/s-2008-1067257
(2008)
Enantioselective Friedel-Crafts alkylation of indole with nitroalkenes in the presence of bifunctional squaramide organocatalysts

Doi:10.1016/j.tetlet.2021.153153
(2021)
Doi:10.1021/ja01939a013
(1909)
Addition of OH and alcohols or amines to -C≡N and -CH=CH₂ groups of CH₂=CHCN coordinated to Cp*Ir(η³-CH₂CHCHPh)

Doi:10.1021/om0002881
(2000)

Article Doi