Literature DB >> 26109330

Conformational and Chiral Properties of Cyclic-tri(N-methyl-meta-benzamide) Bearing Amidino Groups.

Shizuka Nishiyama1, Ko Urushibara1, Hyuma Masu2, Isao Azumaya3, Hiroyuki Kagechika4, Aya Tanatani1.   

Abstract

Cyclic triamides bearing amidino groups at the meta position of the phenyl rings were synthesized, and their conformational properties in the crystal and in solution were examined. Compound exists as a capsule-type dimer of the enantiomers with a bowl-shaped syn conformation in the crystal state. Compound exists mainly in the syn form in solution, and chiral induction was observed upon addition of a chiral acid to a solution of.
© 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  chiral induction; crystal structure; cyclic amide; dimer, capsule

Mesh:

Substances:

Year:  2015        PMID: 26109330     DOI: 10.1002/chir.22476

Source DB:  PubMed          Journal:  Chirality        ISSN: 0899-0042            Impact factor:   2.437


  1 in total

1.  Cylindrical macrocyclic compounds synthesized by connecting two bowl-shaped calix[3]aramide moieties: structures and chiroptical properties.

Authors:  Ryoko Sakagami; Yuuki Saito; Ryuichi Mori; Misa Satake; Misaki Okayasu; Shoko Kikkawa; Hidemasa Hikawa; Isao Azumaya
Journal:  RSC Adv       Date:  2020-09-18       Impact factor: 4.036

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.