
Tetrahedron p. 12679 - 12690 (1997)
Update date:2022-08-04
Topics: Reactivity Chemistry Grignard Reagent Acylal Organolithium reagent
Sydnes, Leiv K.
Sandberg, Marcel
Aldehyde acylals have been prepared and reacted with Grignard and alkyllithium reagents. Acylals from formaldehyde furnished complex reaction mixtures when reacted with both reagents. Acylals of other aldehydes gave reaction mixtures that consisted mainly of an ester, generated by replacing one of the carboxy groups with the organic part of the organometallic reagent, and regenerated aldehyde. The esters were formed in the highest yields. Yields above 90% were experienced when the acylals were reacted with Grignard reagents under Barbier conditions.
View MoreXinjiang Fufeng Biotechnologies Co., Ltd.
Contact:+86-539-7287111
Address:GANQUANPU INDUSTRIAL PARK, ECONOMIC AND TECHNOLOGICAL DEVELOPMENT AREA (TOUTUNHE DISTRICT) OF URUMQI
Huaihua Baohua Biotechnology Co.,Ltd
website:http://www.baochengchem.com
Contact:86-519-82698291
Address:HouYang chemical development zone,Jintan,Jiangsu,China (213200)
Contact:+86 755 26588093
Address:No.9 Linkong West Street, Hengdian Street, Huangpi District, Wuhan City, China.
Contact:0550-7041128 0550-7090578
Address:Wangdian Street,Xinjie Town
suzhou chukai pharmateach co,.ltd
Contact:86-512-88812511
Address:Building 3, Wujiang Scientific Innovation Park, 2358 Changan Rd, Wujiang 215200, Jiangsu Province, P. R. China
Doi:10.1021/jo00813a036
(1971)Doi:10.1021/ol0059955
(2000)Doi:10.1016/S0928-0987(00)00089-0
(2000)Doi:10.1016/0277-5387(96)00100-3
(1996)Doi:10.1021/jm0000113
(2000)Doi:10.1021/jm00288a005
(1971)