70752-22-6Relevant articles and documents
Multiturn Hollow Helices: Synthesis and Folding of Long Aromatic Oligoamides
Ferrand, Yann,Gong, Bing,Huc, Ivan,Kauffmann, Brice,Liu, Rui,Lu, Zhong-Lin,Xu, Wenwu,Zeng, Xiao Cheng,Zhong, Yulong
supporting information, p. 6938 - 6942 (2020/09/15)
Aromatic oligoamides adopting helical conformations are synthesized by coupling carboxyl-terminated basic units having two, four, and eight residues to amine-terminated oligomer precursors. Coupling yields show no noticeable reduction with the size of the
Aromatic oligoamide macrocycles from the bimolecular coupling of folded oligomeric precursors
Yang, Liuqing,Zhong, Lijian,Yamato, Kazuhiro,Zhang, Xiaheng,Feng, Wen,Deng, Pengchi,Yuan, Lihua,Zeng, Xiao Cheng,Gong, Bing
supporting information; experimental part, p. 729 - 733 (2009/06/20)
Aromatic oligoamide macrocycles consisting of six to ten meta-linked residues were prepared based on bimolecular coupling/cyclization of a pentameric diamine and oligomeric diacid chlorides, and adopt folded conformations enforced by intramolecular three-
N-(3-pyrrolidinyl) benzamide derivative
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, (2008/06/13)
N-(3-Pyrrodinyl)benzamide derivatives represented by the following general formula (I) which have potent and selective antagonism against dopamine D3 and/or D4 receptor and are useful as a psychotropic, a schizophrenia-treating agent and the like, or a pharmaceutically acceptable salt thereof or a pharmaceutical preparation thereof. STR1