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Cover Feature: Unusual C 2h ‐Symmetric trans‐ 1‐(Bis‐pyrrolidine)‐tetra‐malonate Hexa‐Adducts of C 60 : The Unexpected Regio‐ and Stereocontrol Mediated by Malonate–Pyrrolidine Interaction (Chem. Eur. J. 63/2017)
Author(s) -
Castro Edison,
Azmani Khalid,
Garcia Andrea Hernandez,
Aghabali Amineh,
Liu Shuming,
MettaMagana Alejandro J.,
Olmstead Marilyn M.,
RodríguezFortea Antonio,
Poblet Josep M.,
Echegoyen Luis
Publication year - 2017
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201703999
Subject(s) - hexa , pyrrolidine , tetra , malonate , adduct , chemistry , cycloaddition , cover (algebra) , stereochemistry , medicinal chemistry , organic chemistry , catalysis , mechanical engineering , engineering
A totally unanticipated regio‐ and stereo‐isomerically pure C 2h ‐symmetric trans‐1 ‐(bis‐pyrrolidine)‐tetra‐malonate hexa‐adduct of C 60 was obtained via a topologically controlled method, followed by a 1,3‐dipolar cycloaddition reaction. The graphic shows the fullerene C 60 in the center and from this many other compounds can be obtained. More information can be found in the Full Paper by M. M. Olmstead, J. M. Poblet, L. Echegoyen et al. on page 15937.