Chemistry of Heterocyclic Compounds p. 15 - 17 (1987)
Update date:2022-08-16
Topics:
Lukevits, E.
Ignatovich, L. M.
Iovel', I. G.
Gol'dberg, Yu. Sh.
Shimanskaya, M. V.
The transformations of trimethyl(5-methyl-2-furyl)silane and trimethyl(5-methyl-2-furyl)germane were studied upon vapor-phase oxidation by atmospheric oxygen on a V-Mo-Ag-O catalyst.Under these conditions, trimethyl(5-formyl-2-furyl)silane and trimethyl(5-formyl-2-furyl)germane are formed albeit in only 5-7percent yield.This low yield is a consequence of the thermal instability of the starting compounds and the aldehydes formed.The oxidation of 2-methyl-5-tert-butylfuran was studied under comparable conditions.The corresponding aldehyde was obtained in 30percent yield.A scheme was proposed for the catalytic oxidation of 5-substituted 2-methylfurans.
View More
A.M FOOD CHEMICAL CO., LIMITED
Contact:86-531-87100375
Address:20Floor，Bblock，1Building，pharma-valley，Jinan，China
Contact:+86-(0)21-3770 9035
Address:Room 301, Building 2, Meijiabang Road 1508, Shanghai China
Jinhua Haoyuan Chemical CO., LTD(expird)
Contact:86-579-82465583
Address:Jinhua,Zhejiang
Chuzhou Baiao Biologhy S&T Co., Ltd.
Contact:+86-25-83212599；+86-25-83212699 13705185959
Address:Room 905, Tianzheng International Platza, No.399, Zhongyang Road ,Nanjing, Jiangsu Province, China
Tianjin Boron PharmaTech Co.,Ltd.(expird)
Contact:86-022-59845187
Address:B9-401, Tianda Science Park,No.80,4th Avenue,TEDA,Tianjin, China
Doi:10.1080/10715762.2020.1808632
(2020)Doi:10.1039/DT9900002743
(1990)Doi:10.1016/0039-128X(83)90096-X
(1983)Doi:10.3390/molecules23030599
(2018)Doi:10.1016/j.electacta.2010.10.022
(2011)Doi:10.1002/jhet.5570430106
(2006)
