Aluminium Triiodide Mediated Reductive Dehalogenation of α-Halocarbonyl Compounds and Trapping of the Aluminium Enolate Intermediate via Aldol Reaction

DOI: 10.1039/c39910000154

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 154 - 155 (1991)

Update date:2022-08-29

Topics:

Authors:

Borah, Harsha N.

Boruah, Romesh C.

Sandhu, Jagir S.

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

Article abstract of DOI:10.1039/c39910000154

Aluminium triiodide has been conveniently used for reductive dehalogenation and aldol condensation of α-halocarbonyl compounds via aluminium enolate.

Full text of DOI:10.1039/c39910000154

View Article Online / Journal Homepage / Table of Contents for this issue

View Article Online

Products guided by the article

Product name:2-(HYDROXY-PHENYL-METHYL)-CYCLOHEXANONE

Cas No:13161-18-7

R&D Labs maybe for 13161-18-7

Sino Rarechem Labs Co.Ltd

Contact:+86-0512-62857507

Address:Boji Science Park, No1688C,Taishan road, Suzhou ,China
Jiangyin Tenghua Import&Export Co.,Ltd.

Contact:+86-510-86263875

Address:Room 402-B,9 Yanling Road, Jiangyin,Jiangsu, China
SHANGHAI RC CHEMICALS CO.,LTD.

website:http://www.rcc.net.cn

Contact:+86-21-50322175

Address:Rm1415 Yinqiao Masion No.58 Jinxin Road Pudong Shanghai China
Wuhan Hanye Chemical New Material Co.,Ltd

Contact:+86-27-85308141

Address:LiuDian, Panlongcheng Economic Development Zone, HuangPi district, Wuhan, Hubei 430311 P.R.China
STAR SYNTHESIS CO.,LIMITED

Contact:+(852) 301-98033

Address:Flat C, 23/F, Lucky Plaza, 315-321 Lockhart Road, Wan Chai, Hong Kong

Relevant to this article

Asymmetric hydrogenation of diethyl 1-phenylvinylphosphonate by metal complexes in CH2Cl2 and in supercritical carbon dioxide using phosphite-type ligands

Doi:10.1007/s11172-014-0493-y
(2014)
An entry to 2-(cyclobut-1-en-1-yl)-1: H -indoles through a cyclobutenylation/deprotection cascade

Doi:10.1039/d1ob00430a
(2021)
Regioselective halogenation of pyridinium N-(benzoazynyl) aminides as a way to produce N-benzyl-α-aminobenzoazines

Doi:10.1016/j.tet.2018.03.064
(2018)
Acyl Donors and Additives for the Biocatalytic Friedel–Crafts Acylation

Doi:10.1002/ejoc.201701079
(2017)
Synthesis and properties of a new AIE macrocyclic emitter with triarylamine backbone

Doi:10.1016/j.tetlet.2017.08.004
(2017)
Atmospheric chemistry of CH₂Br₂: Rate coefficients for its reaction with Cl atoms and OH and the chemistry of the CHBr₂O radical

Doi:10.1002/(SICI)1097-4601(1996)28:6<433::AID-KIN5>3.0.CO;2-W
(1996)

Article Doi