Monatshefte fur Chemie p. 645 - 650 (1985)
Update date:2022-08-05
Topics: Amine Yield NMR spectroscopy Catalyst Chromatography Recrystallization Mass spectrometry (MS) Aldehyde TLC (thin-layer chromatography) HPLC (high-performance liquid chromatography) Protecting group Anhydrous conditions Workup Reductive Amination N-Substitution Stoichiometry Inert atmosphere Solvent extraction pH adjustment
Angrick, Michael
O-Benzyl-N-(benzyloxycarbonyl)-DL-serine methyl ester (1a) and peptides 1b-d with C-terminal O-benzylserine ester have been reduced with diisobutylaluminium hydride to yield the N-substituted aminoglyceraldehydes 2a-d.Using lithium tetrahydridoaluminate as the reducing agent the corresponding alcohols 3a-d have been obtained. - (Keywords: Maillard reaction; N-Substituted aminoglyceraldehydes)
View MoreShandong Bolode Bio-Technology Co., LTD
Contact:+86-0531-58966870
Address:136 Jingyi Road,Huaiyin District,Jinan,Shandong,China
Taimai Sanluck Pharmaceutical Co.,Ltd
Contact:86-592-7662921
Address:8D,No.186,Huarong Road,Huli,Xiamen,China
Hangzhou yi lu biont technology Co., LTD
Contact:+86-571-88152630
Address:Hangzhoushi HuafengRoad Yicheng3Building1001room.
Laohekou Jinghong Chemical Co.,Ltd
Contact:+86-0710-3702747
Address:163.East，Huagong Road，Laohekou
Shanghai Pengkai Chemical Co.,Ltd
Contact:+86-21-60526671
Address:No.4226 Duzhuang Rd Minhang District Shanghai China
Doi:10.1021/ja01352a051
(1931)Doi:10.1016/0022-328X(85)80037-1
(1985)Doi:10.1021/ja01547a025
(1958)Doi:10.1002/hlca.19510340117
(1951)Doi:10.1021/ja01546a023
(1958)Doi:10.1246/cl.1985.579
(1985)
