4.5 Article

Preparation of enantiomerically pure derivatives of (3-amino-1,2-dicarba-closo-dodecaboran-1-yl)acetic acid

Journal

JOURNAL OF ORGANOMETALLIC CHEMISTRY
Volume 876, Issue -, Pages 50-56

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jorganchem.2018.08.018

Keywords

Closo-carborane; Planar chirality; Chiral HPLC; Amino acid; Configuration assignment; X-ray diffraction

Funding

  1. Russian Foundation for Basic Research [16-33-60122]
  2. Ministry of Education and Science of the Russian Federation [AAAA-A18-118020290146-2]

Ask authors/readers for more resources

The enantiomerically pure N- and C-protected derivatives of planar-chiral (3-amino-1,2-dicarba-closo-dodecaboran-1-yl)acetic acid (>99% ee) have first been obtained in good yields via a combination of HPLC separation and synthetic procedures. Assignment of absolute configuration of the carborane fragments has been made based on the X-ray diffraction data of diastereoisomeric derivatives of (S)-amino acids. (C) 2018 Elsevier B.V. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available