A new method for synthesis of functionalized organozinc-copper(I) reagents and their 1,4-addition reaction with enones

DOI: 10.1080/00397919808004854

Source and publish data:

Synthetic Communications p. 2793 - 2800 (1998)

Update date:2022-08-16

Topics:

Authors:

Hu, Yulai

Yu, Jianhua

Yang, Shiyan

Wang, Jin-Xian

Yin, Yuanqi

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

Article abstract of DOI:10.1080/00397919808004854

The transmetalation of functionalized organozinc iodides with Cu(OAc)₂ in THF provides a new convenient method for the preparation of functionalized organozinc-copper(I) reagents FG-RCu(OAc)ZnI which ultimately undergo 1,4- addition reaction wi

Full text of DOI:10.1080/00397919808004854

Synthetic Communications

ISSN: 0039-7911 (Print) 1532-2432 (Online) Journal homepage: http://www.tandfonline.com/loi/lsyc20

A New Method for Synthesis of Functionalized

Organozinc-Copper(I) Reagents and Their 1,4-

Addition Reaction with Enones

Yulai Hu , Jianhua Yu , Shiyan Yang , Jin-Xian Wang & Yuanqi Yin

To cite this article: Yulai Hu , Jianhua Yu , Shiyan Yang , Jin-Xian Wang & Yuanqi Yin (1998)

A New Method for Synthesis of Functionalized Organozinc-Copper(I) Reagents and Their

,4-Addition Reaction with Enones, Synthetic Communications, 28:15, 2793-2800, DOI:

0.1080/00397919808004854

To link to this article: http://dx.doi.org/10.1080/00397919808004854

Published online: 20 Aug 2006.

Submit your article to this journal

Article views: 88

View related articles

Citing articles: 5 View citing articles

Full Terms & Conditions of access and use can be found at

http://www.tandfonline.com/action/journalInformation?journalCode=lsyc20

Download by: ["University at Buffalo Libraries"]

Date: 09 June 2016, At: 13:10

Products guided by the article

Product name:Acetic acid 4-(3-oxo-cyclohexyl)-butyl ester

Cas No:119649-85-3

R&D Labs maybe for 119649-85-3

Chemtrade International ( China )

Contact:+86-532-86893005

Address:Rm 2-501, Huaxia Zonghe Building, No. 410 JInggangshan Road, Huangdao
Wuhan Shengmao Corp

website:http://www.shengmaochem.com

Contact:86-27-82853423, 82819281

Address:Rm 202, A Unit Huaqiao Building No. 2, Lihuangpi Road, Wuhan, China
Liaoyang hengye Chemical Co., Ltd.

Contact:86-419-5850866

Address:North Old Xiaoxiao Road,Yantai District, Dengta, Liaoyang, Liaoning, China
Jiangsu Seed Chem Co.,Ltd.

Contact:86-513-84128750/13773795976

Address:No.48.Youyi West Road ,Rudong Development Zone,Jiangsu Province,China
Hawks Chemical

Contact:+44 (0)161 367 9441

Address:

Relevant to this article

Kinetic parameters of the thermal decomposition of trimethylindium by DSC

Doi:10.1016/s0040-6031(99)00295-6
(1999)
Amino-substituted O⁶-benzyl-5-nitrosopyrimidines: Interplay of molecular, molecular-electronic and supramolecular structures

Doi:10.1107/S0108768101021607
(2002)
Synthesis and multinuclear magnetic resonance study of stereochemically nonrigid derivatives of iron pentacarbonyl containing bidentate ligands

Doi:10.1021/ic50154a017
(1975)
Non-nucleoside inhibitors of the hepatitis C virus NS5B polymerase: Discovery and preliminary SAR of benzimidazole derivatives

Doi:10.1016/j.bmcl.2003.10.023
(2004)
CLAISEN REARRANGEMENTS-XV STRUCTURE REVISION OF THE COUMARIN, CELERIN, BY SYNTHESIS

Doi:10.1016/S0040-4020(01)91276-1
(1984)
Diseleno[2,3-b:3′,2′-d]selenophene and Diseleno[2,3-b:3′,2′-d] thiophene: Building Blocks for the Construction of [7]Helicenes

Doi:10.1021/acs.joc.7b01362
(2017)

Article Doi