Synthesis of novel fullerene α-amino acid conjugates

Jing Zhang Yan Xia Wang Feng Kang Ying Ya Shao Zong Jie Li Xin Lin Yang

引用本文: Jing Zhang,  Yan Xia Wang,  Feng Kang,  Ying Ya Shao,  Zong Jie Li,  Xin Lin Yang. Synthesis of novel fullerene α-amino acid conjugates[J]. Chinese Chemical Letters, 2008, 19(10): 1159-1162. doi: 10.1016/j.cclet.2008.06.035 shu
Citation:  Jing Zhang,  Yan Xia Wang,  Feng Kang,  Ying Ya Shao,  Zong Jie Li,  Xin Lin Yang. Synthesis of novel fullerene α-amino acid conjugates[J]. Chinese Chemical Letters, 2008, 19(10): 1159-1162. doi: 10.1016/j.cclet.2008.06.035 shu

Synthesis of novel fullerene α-amino acid conjugates

  • 基金项目:

    This work is supported by the National Natural Science foundation of China (No. 20672012).

摘要: Aspartie acid and glutamic acid with protected α-amino and α-carboxyl groups had been used to react with the activated hydroxyl group of N-substituted 3,4-fuUero pyrrolidine.The products were deprotected,affording two monofullerene α-amino acids,monofullerene aspartic acid(mFas) and monofullerene glutamic acid(mFgu).Then a bifullerene glutamic acid conjugate (bFguC)was synthesized by reaction of mFgu containing protected amino group with N-subsfimted 3,4-fullero pyrrolidine.

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  • 收稿日期:  2008-03-20
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