
Journal of Organic Chemistry p. 5841 - 5844 (1992)
Update date:2022-08-04
Topics:
Choudary, Boyapati M.
Prasad, Annavajhula Durga
Bhuma, Vendantam
Swapna, Vinukonda
A mild and efficient method for benzylic oxidation of arylmethylenes to the corresponding carbonyl compounds in good yields is described using a catalytic amount of chromium-pillared montmorillonite and equimolar quantities of tert-butyl hydroperoxide.The method is very selective toward monocarbonyl compounds of the substrates prone to form dicarbonyl compounds.The present heterogeneous catalyst is inert toward the branched hydrocarbone and has been put to practice to obtain p-isobutylacetophenone selectively from p-isobutylethylbenzene.Further, the method is extended successfully to the oxidative debenzylation reactions for the first time.A striking feature of the oxidative deprotection with the present method is the deprotection of a benzyl group from the substrates having any alkyne moiety.
View MoreLanzhou huibang biological chemical technology Co., LTD
Contact:0931-7843964
Address:NO.2011,Yannan Road,Chengguan,
website:http://www.alwaychem.com
Contact:+86-532-8586-4000, 8586-5000
Address:NO.51, TAIPING ROAD, QINGDAO, CHINA. 266001
Hangzhou Yingshanhua Pigment Chemicals Co.,Ltd.
Contact:+86-0150-58101658
Address:Nanyang Economic DevelopmentZong,Xiaoshan,Hangzhou,China
WUXI KINGHAN BIO-MEDICAL&CHEMICAL INC.
Contact:13861062998
Address:Room 1316,No.1619 Huishan Avenue,Wuxi,China
Taizhou Green Peptide Trading Co., Ltd.
Contact:--15314709780
Address:Room 1501, No71, Yuehe Road, Taizhou City, Zhejiang Province, China
Doi:10.1016/j.bmc.2013.03.070
(2013)Doi:10.1002/anie.201207206
()Doi:10.1016/S0040-4039(00)74683-1
(1992)Doi:10.1039/c3cc42365d
(2013)Doi:10.1021/ja00047a018
(1992)Doi:10.1021/jo400440z
(2013)