Journal
JOURNAL OF ORGANOMETALLIC CHEMISTRY
Volume 876, Issue -, Pages 50-56Publisher
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
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Funding
- Russian Foundation for Basic Research [16-33-60122]
- Ministry of Education and Science of the Russian Federation [AAAA-A18-118020290146-2]
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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.
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