利用α-氨基、α-羧基均被保护的天冬氨酸或谷氨酸的非α-羧基与中间体N-取代的3,4-富勒烯吡咯烷衍生物的活化羟基进行缩合反应,产物脱保护后得到了2种新的α-富勒烯氨基酸:富勒烯天冬氨酸和富勒烯谷氨酸.采用MALDI-TOF质谱、红外光谱、紫外可见光谱、1HNMR等方法对它们进行了结构表征.合成的新型富勒烯氨基酸含有游离的氨基、羧基,具有独特的化学结构和性质,在生物医学领域具有潜在的应用前景.
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