作者:V. V. Rozhkov、V. N. Voznesenskii、R. G. Kostyanovsky
DOI:10.1007/bf02495517
日期:1998.1
The possibility of tranferring chirality from nitrogen to carbon by a three-step transformation of racemic dimethyl 1-methoxyaziridine-2,2-dicarboxylate into 3-amino-2-chloromethyl-2-methoxyaminopropan-1-ol was demonstrated. The first representative of 1-silyloxyaziridines,viz., dimethyl 1-(tert-butyldimethylsilyloxy)aziridine-2,2-dicarboxylate, was synthesized by acidolysis or thermolysis of triazoline
证明了通过将外消旋二甲基 1-甲氧基氮丙啶-2,2-二甲酸二甲酯三步转化为 3-氨基-2-氯甲基-2-甲氧基氨基丙-1-醇,将手性从氮转移到碳的可能性。1-甲硅烷氧基氮丙啶的第一个代表,即1-(叔丁基二甲基甲硅烷氧基)氮丙啶-2,2-二甲酸二甲酯,是通过三唑啉的酸解或热解合成的,三唑啉是由间草酸二甲酯的叔丁基二甲基甲硅烷基肟与CH2N2反应得到的